Linked Data
dbSNP Id:
rs753244751
ExAC:
1:209974661 G / C
gnomAD v2:
1-209974661-G-C
gnomAD v4:
1-209801316-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.209801316G>C , CM000663.2:g.209801316G>C | GRCh38 |
| NC_000001.10:g.209974661G>C , CM000663.1:g.209974661G>C | GRCh37 |
| NC_000001.9:g.208041284G>C | NCBI36 |
| NG_007081.2:g.9819C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696133.1:c.98C>G | ENSP00000512426.1:p.Ser33Cys | |
| ENST00000696134.1:c.98C>G | ENSP00000512427.1:p.Ser33Cys | |
| ENST00000367021.8:c.98C>G MANE Select | ENSP00000355988.3:p.Ser33Cys | |
| ENST00000643798.1:c.98C>G | ENSP00000496669.1:p.Ser33Cys | |
| ENST00000367021.7:c.98C>G | ENSP00000355988.3:p.Ser33Cys | |
| ENST00000456314.1:c.98C>G | ENSP00000403855.1:p.Ser33Cys | |
| ENST00000542854.5:c.-112+4631C>G | ENSP00000440532.1:n.-112+4631C>G | |
| NM_001206696.1:c.-112+4631C>G | NP_001193625.1:n.-112+4631C>G | |
| NM_006147.3:c.98C>G | NP_006138.1:p.Ser33Cys | |
| NM_006147.4:c.98C>G MANE Select | NP_006138.1:p.Ser33Cys | |
| NM_001206696.2:c.-112+4631C>G | NP_001193625.1:n.-112+4631C>G |