Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.61992400T= , CM000672.2:g.61992400T= | GRCh38 |
| NC_000010.10:g.63752159T= , CM000672.1:g.63752159T= | GRCh37 |
| NC_000010.9:g.63422165T= | NCBI36 |
| NG_030027.1:g.96147T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_032199.3:c.503-7691T= MANE Select | NP_115575.1:n.503-7691T= |
| ENST00000279873.12:c.503-7691T= MANE Select | ENSP00000279873.7:n.503-7691T= |
| NM_032199.2:c.503-7691T= | NP_115575.1:n.503-7691T= |
| ENST00000279873.11:c.503-7691T= | ENSP00000279873.7:n.503-7691T= |
| ENST00000644638.1:c.503-7691T= | ENSP00000494412.1:n.503-7691T= |
| ENST00000681100.1:c.503-7691T= | ENSP00000506119.1:n.503-7691T= |
| XM_011540262.1:c.502+51992T= | XP_011538564.1:n.502+51992T= |
| XM_024448230.1:c.-65-7691T= | XP_024303998.1:n.-65-7691T= |