Linked Data
ClinVar Variation Id:
162585
dbSNP Id:
rs200024875
ExAC:
22:33670429 G / C
gnomAD v2:
22-33670429-G-C
gnomAD v3:
22-33274443-G-C
gnomAD v4:
22-33274443-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.33274443G>C , CM000684.2:g.33274443G>C | GRCh38 |
| NC_000022.10:g.33670429G>C , CM000684.1:g.33670429G>C | GRCh37 |
| NC_000022.9:g.32000429G>C | NCBI36 |
| NG_009929.2:g.650986C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354992.7:c.2255C>G | ENSP00000347088.2:p.Ala752Gly | |
| ENST00000397394.8:c.2255C>G MANE Select | ENSP00000380549.2:p.Ala752Gly | |
| ENST00000402320.6:c.2099C>G | ENSP00000385223.1:p.Ala700Gly | |
| ENST00000413114.6:c.2255C>G | ENSP00000415546.2:p.Ala752Gly | |
| ENST00000608642.6:c.1730+29786C>G | ENSP00000476866.2:n.1730+29786C>G | |
| ENST00000609799.6:c.1451+41642C>G | ENSP00000476415.2:n.1451+41642C>G | |
| ENST00000610186.6:c.1877+8759C>G | ENSP00000476364.2:n.1877+8759C>G | |
| ENST00000674543.1:c.*1696C>G | ENSP00000501590.1:n.*1696C>G | |
| ENST00000674668.1:c.2129C>G | ENSP00000502103.1:p.Ala710Gly | |
| ENST00000674708.1:n.1913C>G | ||
| ENST00000674780.1:c.1652C>G | ENSP00000502772.1:p.Ala551Gly | |
| ENST00000674789.1:c.2108C>G | ENSP00000501941.1:p.Ala703Gly | |
| ENST00000674816.1:n.2063C>G | ||
| ENST00000674999.1:c.2051C>G | ENSP00000502711.1:p.Ala684Gly | |
| ENST00000675277.1:c.2051C>G | ENSP00000502702.1:p.Ala684Gly | |
| ENST00000675382.1:c.*693C>G | ENSP00000501800.1:n.*693C>G | |
| ENST00000675416.1:c.2255C>G | ENSP00000502826.1:p.Ala752Gly | |
| ENST00000676031.1:c.*837C>G | ENSP00000501663.1:n.*837C>G | |
| ENST00000676070.1:c.2255C>G | ENSP00000502152.1:p.Ala752Gly | |
| ENST00000676126.1:c.1976C>G | ENSP00000501966.1:p.Ala659Gly | |
| ENST00000676132.1:c.2255C>G | ENSP00000501854.1:p.Ala752Gly | |
| ENST00000676370.1:c.2255C>G | ENSP00000502238.1:p.Ala752Gly | |
| ENST00000354992.6:c.2255C>G | ENSP00000347088.2:p.Ala752Gly | |
| ENST00000397394.6:c.2255C>G | ENSP00000380549.2:p.Ala752Gly | |
| ENST00000402320.5:c.2099C>G | ENSP00000385223.1:p.Ala700Gly | |
| ENST00000608642.5:c.761+29786C>G | ENSP00000476866.1:n.761+29786C>G | |
| ENST00000609799.5:c.482+41642C>G | ENSP00000476415.1:n.482+41642C>G | |
| ENST00000610186.5:c.908+8759C>G | ENSP00000476364.1:n.908+8759C>G | |
| NM_004737.4:c.2255C>G | NP_004728.1:p.Ala752Gly | |
| NM_133642.3:c.2255C>G | NP_598397.1:p.Ala752Gly | |
| XM_005261831.2:c.2255C>G | XP_005261888.1:p.Ala752Gly | |
| XM_005261832.2:c.2255C>G | XP_005261889.1:p.Ala752Gly | |
| XM_011530510.1:c.2255C>G | XP_011528812.1:p.Ala752Gly | |
| XM_011530511.1:c.1976C>G | XP_011528813.1:p.Ala659Gly | |
| XM_011530512.1:c.1652C>G | XP_011528814.1:p.Ala551Gly | |
| XM_011530513.1:c.1157C>G | XP_011528815.1:p.Ala386Gly | |
| NM_001362949.1:c.2255C>G | NP_001349878.1:p.Ala752Gly | |
| NM_001362951.1:c.2255C>G | NP_001349880.1:p.Ala752Gly | |
| NM_001362953.1:c.2255C>G | NP_001349882.1:p.Ala752Gly | |
| NM_004737.6:c.2255C>G | NP_004728.1:p.Ala752Gly | |
| NM_133642.4:c.2255C>G | NP_598397.1:p.Ala752Gly | |
| XM_005261831.3:c.2255C>G | XP_005261888.1:p.Ala752Gly | |
| XM_005261832.3:c.2255C>G | XP_005261889.1:p.Ala752Gly | |
| XM_011530512.2:c.1652C>G | XP_011528814.1:p.Ala551Gly | |
| XM_011530513.2:c.1157C>G | XP_011528815.1:p.Ala386Gly | |
| XM_024452302.1:c.1877+8759C>G | XP_024308070.1:n.1877+8759C>G | |
| XR_002958722.1:n.1924+8759C>G | ||
| NM_001362949.2:c.2255C>G | NP_001349878.1:p.Ala752Gly | |
| NM_001362951.2:c.2255C>G | NP_001349880.1:p.Ala752Gly | |
| NM_001362953.2:c.2255C>G | NP_001349882.1:p.Ala752Gly | |
| NM_001378624.1:c.2255C>G | NP_001365553.1:p.Ala752Gly | |
| NM_001378625.1:c.2255C>G | NP_001365554.1:p.Ala752Gly | |
| NM_001378626.1:c.2255C>G | NP_001365555.1:p.Ala752Gly | |
| NM_001378627.1:c.2108C>G | NP_001365556.1:p.Ala703Gly | |
| NM_001378628.1:c.2108C>G | NP_001365557.1:p.Ala703Gly | |
| NM_001378629.1:c.2099C>G | NP_001365558.1:p.Ala700Gly | |
| NM_001378630.1:c.1652C>G | NP_001365559.1:p.Ala551Gly | |
| NM_001378631.1:c.1349C>G | NP_001365560.1:p.Ala450Gly | |
| NM_004737.7:c.2255C>G | NP_004728.1:p.Ala752Gly | |
| NM_133642.5:c.2255C>G MANE Select | NP_598397.1:p.Ala752Gly |