Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215671229G>A , CM000663.2:g.215671229G>A | GRCh38 |
| NC_000001.10:g.215844571G>A , CM000663.1:g.215844571G>A | GRCh37 |
| NC_000001.9:g.213911194G>A | NCBI36 |
| NG_009497.1:g.757168C>T | |
| NG_009497.2:g.757220C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.13876C>T MANE Select | ENSP00000305941.3:p.Gln4626Ter | |
| ENST00000674083.1:c.13876C>T | ENSP00000501296.1:p.Gln4626Ter | |
| ENST00000307340.7:c.13876C>T | ENSP00000305941.3:p.Gln4626Ter | |
| NM_206933.2:c.13876C>T | NP_996816.2:p.Gln4626Ter | |
| NM_206933.3:c.13876C>T | NP_996816.2:p.Gln4626Ter | |
| NM_206933.4:c.13876C>T MANE Select | NP_996816.3:p.Gln4626Ter |