Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.20164512A= , CM000669.2:g.20164512A= | GRCh38 |
| NC_000007.13:g.20204135A= , CM000669.1:g.20204135A= | GRCh37 |
| NC_000007.12:g.20170660A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000400331.10:c.-152-113T= MANE Select | ENSP00000383185.3:n.-152-113T= | |
| ENST00000332878.8:c.-8-2642T= | ENSP00000328410.4:n.-8-2642T= | |
| ENST00000400331.9:c.-152-113T= | ENSP00000383185.3:n.-152-113T= | |
| ENST00000471019.1:n.274-113T= | ||
| ENST00000589011.1:c.-8-2642T= | ENSP00000466864.1:n.-8-2642T= | |
| NM_182762.3:c.-152-113T= | NP_877439.3:n.-152-113T= | |
| NM_182762.4:c.-152-113T= MANE Select | NP_877439.3:n.-152-113T= |