Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73404276C>T , CM000666.2:g.73404276C>T | GRCh38 |
| NC_000004.11:g.74269993C>T , CM000666.1:g.74269993C>T | GRCh37 |
| NC_000004.10:g.74488857C>T | NCBI36 |
| NG_009291.1:g.5022C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000477.5:c.-52C>T | NP_000468.1:n.-52C>T |
| NM_000477.6:c.-52C>T | NP_000468.1:n.-52C>T |
| ENST00000295897.8:c.-52C>T | ENSP00000295897.4:n.-52C>T |
| ENST00000441319.5:c.48-93C>T | ENSP00000392541.1:n.48-93C>T |
| ENST00000621628.4:c.-52C>T | ENSP00000480485.1:n.-52C>T |