Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.74689126T= , CM000667.2:g.74689126T= | GRCh38 |
| NC_000005.9:g.73984951T= , CM000667.1:g.73984951T= | GRCh37 |
| NC_000005.8:g.74020707T= | NCBI36 |
| NG_009770.1:g.8983T= | |
| NG_009770.2:g.54104T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261416.12:c.300-202T= MANE Select | ENSP00000261416.7:n.300-202T= | |
| ENST00000261416.11:c.300-202T= | ENSP00000261416.7:n.300-202T= | |
| ENST00000511181.5:c.-376-202T= | ENSP00000426285.1:n.-376-202T= | |
| ENST00000513079.5:n.365-202T= | ||
| ENST00000515528.1:n.355-202T= | ||
| NM_000521.3:c.300-202T= | NP_000512.1:n.300-202T= | |
| NM_001292004.1:c.-376-202T= | NP_001278933.1:n.-376-202T= | |
| NM_000521.4:c.300-202T= MANE Select | NP_000512.2:n.300-202T= | |
| NM_001292004.2:c.-376-202T= | NP_001278933.1:n.-376-202T= |