Linked Data
dbSNP Id:
rs749373145
ExAC:
12:57501050 T / C
gnomAD v2:
12-57501050-T-C
gnomAD v4:
12-57107267-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57107267T>C , CM000674.2:g.57107267T>C | GRCh38 |
| NC_000012.11:g.57501050T>C , CM000674.1:g.57501050T>C | GRCh37 |
| NC_000012.10:g.55787317T>C | NCBI36 |
| NG_021272.1:g.9147A>G | |
| NG_021272.2:g.29873A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300134.8:c.303A>G MANE Select | ENSP00000300134.3:p.Gln101= | |
| ENST00000553533.2:c.303A>G | ENSP00000451546.2:p.Gln101= | |
| ENST00000554764.6:c.*47A>G | ENSP00000451909.1:n.*47A>G | |
| ENST00000640254.2:c.303A>G | ENSP00000491116.2:p.Gln101= | |
| ENST00000651176.1:c.303A>G | ENSP00000498693.1:p.Gln101= | |
| ENST00000300134.7:c.303A>G | ENSP00000300134.3:p.Gln101= | |
| ENST00000454075.7:c.303A>G | ENSP00000401486.3:p.Gln101= | |
| ENST00000537215.6:c.-28A>G | ENSP00000444530.2:n.-28A>G | |
| ENST00000538913.6:c.-28A>G | ENSP00000445409.2:n.-28A>G | |
| ENST00000543873.6:c.303A>G | ENSP00000438451.2:p.Gln101= | |
| ENST00000553397.5:c.303A>G | ENSP00000452203.1:p.Gln101= | |
| ENST00000553499.5:c.303A>G | ENSP00000451074.1:p.Gln101= | |
| ENST00000554663.5:c.303A>G | ENSP00000450665.1:p.Gln101= | |
| ENST00000554764.5:c.*47A>G | ENSP00000451909.1:n.*47A>G | |
| ENST00000554825.5:c.303A>G | ENSP00000451209.1:p.Gln101= | |
| ENST00000555104.5:c.*47A>G | ENSP00000450510.1:n.*47A>G | |
| ENST00000555641.1:n.308A>G | ||
| ENST00000555849.5:c.303A>G | ENSP00000452394.1:p.Gln101= | |
| ENST00000556155.5:c.303A>G | ENSP00000451742.1:p.Gln101= | |
| ENST00000556259.5:c.249A>G | ENSP00000452373.1:p.Gln83= | |
| NM_001178078.1:c.303A>G | NP_001171549.1:p.Gln101= | |
| NM_001178079.1:c.303A>G | NP_001171550.1:p.Gln101= | |
| NM_001178080.1:c.-28A>G | NP_001171551.1:n.-28A>G | |
| NM_001178081.1:c.-28A>G | NP_001171552.1:n.-28A>G | |
| NM_003153.4:c.303A>G | NP_003144.3:p.Gln101= | |
| NR_033659.1:n.470A>G | ||
| XM_006719574.1:c.303A>G | XP_006719637.1:p.Gln101= | |
| XM_006719575.1:c.303A>G | XP_006719638.1:p.Gln101= | |
| XM_011538703.1:c.303A>G | XP_011537005.1:p.Gln101= | |
| XM_011538704.1:c.303A>G | XP_011537006.1:p.Gln101= | |
| XM_011538705.1:c.303A>G | XP_011537007.1:p.Gln101= | |
| XM_011538706.1:c.303A>G | XP_011537008.1:p.Gln101= | |
| XM_011538707.1:c.303A>G | XP_011537009.1:p.Gln101= | |
| XM_011538708.1:c.-28A>G | XP_011537010.1:n.-28A>G | |
| XM_011538709.1:c.-28A>G | XP_011537011.1:n.-28A>G | |
| XM_011538703.3:c.303A>G | XP_011537005.1:p.Gln101= | |
| XM_011538704.3:c.303A>G | XP_011537006.1:p.Gln101= | |
| XM_011538705.3:c.303A>G | XP_011537007.1:p.Gln101= | |
| XM_011538707.3:c.303A>G | XP_011537009.1:p.Gln101= | |
| XM_011538708.3:c.-28A>G | XP_011537010.1:n.-28A>G | |
| NM_003153.5:c.303A>G MANE Select | NP_003144.3:p.Gln101= | |
| NM_001178078.2:c.303A>G | NP_001171549.1:p.Gln101= | |
| NM_001178079.2:c.303A>G | NP_001171550.1:p.Gln101= | |
| NM_001178080.2:c.-28A>G | NP_001171551.1:n.-28A>G | |
| NM_001178081.2:c.-28A>G | NP_001171552.1:n.-28A>G | |
| NR_033659.2:n.419A>G |