Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.73386075C>T , CM000664.2:g.73386075C>T | GRCh38 |
| NC_000002.11:g.73613203C>T , CM000664.1:g.73613203C>T | GRCh37 |
| NC_000002.10:g.73466711C>T | NCBI36 |
| NG_011690.1:g.5321C>T , LRG_741:g.5321C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001378454.1:c.207C>T MANE Select | NP_001365383.1:p.Asp69= |
| ENST00000613296.6:c.207C>T MANE Select | ENSP00000482968.1:p.Asp69= |
| NM_015120.4:c.210C>T , LRG_741t1:c.210C>T | NP_055935.4:p.Asp70= |
| ENST00000484298.5:c.207C>T | ENSP00000478155.1:p.Asp69= |
| ENST00000613296.4:c.207C>T | ENSP00000482968.1:p.Asp69= |
| ENST00000614410.4:c.207C>T | ENSP00000479094.1:p.Asp69= |
| ENST00000682675.1:n.167C>T | |
| ENST00000682889.1:n.172C>T | |
| ENST00000684148.1:n.79C>T |