Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.120737043G>T , CM000674.2:g.120737043G>T | GRCh38 |
| NC_000012.11:g.121174846G>T , CM000674.1:g.121174846G>T | GRCh37 |
| NC_000012.10:g.119659229G>T | NCBI36 |
| NG_007991.1:g.16276G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000242592.9:c.268G>T MANE Select | ENSP00000242592.4:p.Gly90Cys | |
| ENST00000242592.8:c.268G>T | ENSP00000242592.4:p.Gly90Cys | |
| ENST00000411593.2:c.268G>T | ENSP00000401045.2:p.Gly90Cys | |
| ENST00000539690.1:n.380G>T | ||
| NM_000017.3:c.268G>T | NP_000008.1:p.Gly90Cys | |
| NM_001302554.1:c.268G>T | NP_001289483.1:p.Gly90Cys | |
| NM_000017.4:c.268G>T MANE Select | NP_000008.1:p.Gly90Cys | |
| NM_001302554.2:c.268G>T | NP_001289483.1:p.Gly90Cys |