Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.74689132T= , CM000667.2:g.74689132T= | GRCh38 |
| NC_000005.9:g.73984957T= , CM000667.1:g.73984957T= | GRCh37 |
| NC_000005.8:g.74020713T= | NCBI36 |
| NG_009770.1:g.8989T= | |
| NG_009770.2:g.54110T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261416.12:c.300-196T= MANE Select | ENSP00000261416.7:n.300-196T= | |
| ENST00000261416.11:c.300-196T= | ENSP00000261416.7:n.300-196T= | |
| ENST00000511181.5:c.-376-196T= | ENSP00000426285.1:n.-376-196T= | |
| ENST00000513079.5:n.365-196T= | ||
| ENST00000515528.1:n.355-196T= | ||
| NM_000521.3:c.300-196T= | NP_000512.1:n.300-196T= | |
| NM_001292004.1:c.-376-196T= | NP_001278933.1:n.-376-196T= | |
| NM_000521.4:c.300-196T= MANE Select | NP_000512.2:n.300-196T= | |
| NM_001292004.2:c.-376-196T= | NP_001278933.1:n.-376-196T= |