Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154321150T= , CM000663.2:g.154321150T= | GRCh38 |
| NC_000001.10:g.154293626T= , CM000663.1:g.154293626T= | GRCh37 |
| NC_000001.9:g.152560250T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_080429.3:c.-6T= MANE Select | NP_536354.2:n.-6T= |
| ENST00000324978.8:c.-6T= MANE Select | ENSP00000318355.3:n.-6T= |
| NM_080429.2:c.-6T= | NP_536354.2:n.-6T= |
| ENST00000324978.7:c.-6T= | ENSP00000318355.3:n.-6T= |
| ENST00000355197.4:n.61T= | |
| ENST00000484864.1:c.-6T= | ENSP00000420341.1:n.-6T= |
| XM_011510104.1:c.-6T= | XP_011508406.1:n.-6T= |
| XM_011510104.2:c.-6T= | XP_011508406.1:n.-6T= |