Linked Data
dbSNP Id:
rs61731498
ExAC:
1:230846592 C / A
gnomAD v2:
1-230846592-C-A
gnomAD v3:
1-230710846-C-A
gnomAD v4:
1-230710846-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.230710846C>A , CM000663.2:g.230710846C>A | GRCh38 |
| NC_000001.10:g.230846592C>A , CM000663.1:g.230846592C>A | GRCh37 |
| NC_000001.9:g.228913215C>A | NCBI36 |
| NG_008836.1:g.8745G>T | |
| NG_008836.2:g.8745G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366667.6:c.-23G>T MANE Select | ENSP00000355627.5:n.-23G>T | |
| ENST00000679684.1:c.-23G>T | ENSP00000505981.1:n.-23G>T | |
| ENST00000679738.1:c.-23G>T | ENSP00000505063.1:n.-23G>T | |
| ENST00000679802.1:c.-23G>T | ENSP00000505184.1:n.-23G>T | |
| ENST00000679854.1:n.489G>T | ||
| ENST00000679957.1:c.-23G>T | ENSP00000506646.1:n.-23G>T | |
| ENST00000680041.1:c.-23G>T | ENSP00000504866.1:n.-23G>T | |
| ENST00000680783.1:c.-23G>T | ENSP00000506329.1:n.-23G>T | |
| ENST00000681269.1:c.-23G>T | ENSP00000505985.1:n.-23G>T | |
| ENST00000681347.1:n.489G>T | ||
| ENST00000681514.1:c.-23G>T | ENSP00000505963.1:n.-23G>T | |
| ENST00000681772.1:c.-23G>T | ENSP00000505829.1:n.-23G>T | |
| ENST00000366667.4:c.5G>T | ENSP00000355627.4:p.Arg2Leu | |
| NM_000029.3:c.5G>T | NP_000020.1:p.Arg2Leu | |
| NM_000029.4:c.5G>T | NP_000020.1:p.Arg2Leu | |
| NM_001382817.3:c.-23G>T | NP_001369746.2:n.-23G>T | |
| NM_001384479.1:c.-23G>T MANE Select | NP_001371408.1:n.-23G>T |