Linked Data
dbSNP Id:
rs764739866
ExAC:
17:44116558 G / C
gnomAD v2:
17-44116558-G-C
gnomAD v4:
17-46039192-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.46039192G>C , CM000679.2:g.46039192G>C | GRCh38 |
| NC_000017.10:g.44116558G>C , CM000679.1:g.44116558G>C | GRCh37 |
| NC_000017.9:g.41472405G>C | NCBI36 |
| NG_032784.1:g.191183C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432791.7:c.2227C>G MANE Select | ENSP00000387393.3:p.Pro743Ala | |
| ENST00000572904.6:c.2227C>G | ENSP00000461484.1:p.Pro743Ala | |
| ENST00000573286.2:n.3910C>G | ||
| ENST00000574590.6:c.2227C>G | ENSP00000461812.2:p.Pro743Ala | |
| ENST00000575318.6:c.2204-506C>G | ENSP00000461299.1:n.2204-506C>G | |
| ENST00000638275.1:c.2204-506C>G | ENSP00000492576.1:n.2204-506C>G | |
| ENST00000639150.1:c.961C>G | ENSP00000491906.1:p.Pro321Ala | |
| ENST00000639531.1:c.2204-506C>G | ENSP00000491765.1:n.2204-506C>G | |
| ENST00000639853.1:c.1375-506C>G | ||
| ENST00000640636.1:c.346-506C>G | ||
| ENST00000648792.1:c.2227C>G | ENSP00000497628.1:p.Pro743Ala | |
| ENST00000262419.10:c.2227C>G | ENSP00000262419.6:p.Pro743Ala | |
| ENST00000432791.5:c.2227C>G | ENSP00000387393.2:p.Pro743Ala | |
| ENST00000572218.5:n.6444C>G | ||
| ENST00000572679.1:n.359C>G | ||
| ENST00000572904.5:c.2227C>G | ENSP00000461484.1:p.Pro743Ala | |
| ENST00000573286.1:n.83C>G | ||
| ENST00000574590.5:c.2227C>G | ENSP00000461812.1:p.Pro743Ala | |
| ENST00000575318.5:c.2204-506C>G | ENSP00000461299.1:n.2204-506C>G | |
| ENST00000576870.5:n.365-506C>G | ||
| NM_001193465.1:c.2227C>G | NP_001180394.1:p.Pro743Ala | |
| NM_001193466.1:c.2227C>G | NP_001180395.1:p.Pro743Ala | |
| NM_015443.3:c.2227C>G | NP_056258.1:p.Pro743Ala | |
| XM_006721823.1:c.2227C>G | XP_006721886.1:p.Pro743Ala | |
| XM_006721824.2:c.2227C>G | XP_006721887.1:p.Pro743Ala | |
| XM_011524628.1:c.2227C>G | XP_011522930.1:p.Pro743Ala | |
| XM_011524629.1:c.2125C>G | XP_011522931.1:p.Pro709Ala | |
| XM_011524630.1:c.2204-506C>G | XP_011522932.1:n.2204-506C>G | |
| XM_011524631.1:c.2204-506C>G | XP_011522933.1:n.2204-506C>G | |
| XM_011524632.1:c.997C>G | XP_011522934.1:p.Pro333Ala | |
| XM_006721823.2:c.2227C>G | XP_006721886.1:p.Pro743Ala | |
| XM_006721824.4:c.2227C>G | XP_006721887.1:p.Pro743Ala | |
| XM_011524628.3:c.2227C>G | XP_011522930.1:p.Pro743Ala | |
| XM_011524629.3:c.2125C>G | XP_011522931.1:p.Pro709Ala | |
| XM_011524630.3:c.2204-506C>G | XP_011522932.1:n.2204-506C>G | |
| XM_011524631.3:c.2204-506C>G | XP_011522933.1:n.2204-506C>G | |
| XM_011524632.3:c.997C>G | XP_011522934.1:p.Pro333Ala | |
| XM_017024488.2:c.2204-506C>G | XP_016879977.1:n.2204-506C>G | |
| XM_017024489.1:c.2125C>G | XP_016879978.1:p.Pro709Ala | |
| NM_001193466.2:c.2227C>G | NP_001180395.1:p.Pro743Ala | |
| NM_015443.4:c.2227C>G MANE Select | NP_056258.1:p.Pro743Ala | |
| NM_001193465.2:c.2227C>G | NP_001180394.1:p.Pro743Ala | |
| NM_001379198.1:c.2227C>G | NP_001366127.1:p.Pro743Ala |