Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.96143928C>A , CM000670.2:g.96143928C>A | GRCh38 |
| NC_000008.10:g.97156156C>A , CM000670.1:g.97156156C>A | GRCh37 |
| NC_000008.9:g.97225332C>A | NCBI36 |
| NG_008981.1:g.21865G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000287020.7:c.*635G>T MANE Select | ENSP00000287020.4:n.*635G>T | |
| ENST00000287020.6:c.*635G>T | ENSP00000287020.4:n.*635G>T | |
| NM_001001557.2:c.*635G>T | NP_001001557.1:n.*635G>T | |
| XM_011517030.1:c.*635G>T | XP_011515332.1:n.*635G>T | |
| NM_001001557.3:c.*635G>T | NP_001001557.1:n.*635G>T | |
| NM_001001557.4:c.*635G>T MANE Select | NP_001001557.1:n.*635G>T |