Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48965347C= , CM000681.2:g.48965347C= | GRCh38 |
| NC_000019.9:g.49468604C= , CM000681.1:g.49468604C= | GRCh37 |
| NC_000019.8:g.54160416C= | NCBI36 |
| NG_008152.1:g.5039C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000146.4:c.-161C= MANE Select | NP_000137.2:n.-161C= |
| ENST00000331825.11:c.-161C= MANE Select | ENSP00000366525.2:n.-161C= |
| NM_000146.3:c.-161C= | NP_000137.2:n.-161C= |
| ENST00000331825.10:c.-161C= | ENSP00000366525.2:n.-161C= |
| ENST00000622577.2:c.-161C= | ENSP00000484043.1:n.-161C= |
| XM_024451447.1:c.350C= | XP_024307215.1:p.Thr117= |