Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.45803993C>T , CM000681.2:g.45803993C>T | GRCh38 |
| NC_000019.9:g.46307251C>T , CM000681.1:g.46307251C>T | GRCh37 |
| NC_000019.8:g.50999091C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221538.8:c.1653+259G>A MANE Select | ENSP00000221538.2:n.1653+259G>A | |
| ENST00000221538.7:c.1653+259G>A | ENSP00000221538.2:n.1653+259G>A | |
| ENST00000597055.1:c.1653+259G>A | ENSP00000472630.1:n.1653+259G>A | |
| ENST00000600188.5:c.861+259G>A | ENSP00000471559.1:n.861+259G>A | |
| NM_030785.3:c.1653+259G>A | NP_110412.1:n.1653+259G>A | |
| XM_011527351.1:c.1653+259G>A | XP_011525653.1:n.1653+259G>A | |
| XM_011527351.2:c.1653+259G>A | XP_011525653.1:n.1653+259G>A | |
| NM_030785.4:c.1653+259G>A MANE Select | NP_110412.1:n.1653+259G>A |