Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.80273862G>A , CM000672.2:g.80273862G>A | GRCh38 |
| NC_000010.10:g.82033618G>A , CM000672.1:g.82033618G>A | GRCh37 |
| NC_000010.9:g.82023598G>A | NCBI36 |
| NG_008083.1:g.20817C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372213.8:c.1107C>T MANE Select | ENSP00000361287.3:p.Pro369= | |
| ENST00000372213.7:c.1107C>T | ENSP00000361287.3:p.Pro369= | |
| ENST00000480845.1:n.339C>T | ||
| ENST00000485270.5:n.619C>T | ||
| NM_000429.2:c.1107C>T | NP_000420.1:p.Pro369= | |
| XM_005269842.3:c.1107C>T | XP_005269899.1:p.Pro369= | |
| XM_005269843.3:c.984C>T | XP_005269900.1:p.Pro328= | |
| NM_000429.3:c.1107C>T MANE Select | NP_000420.1:p.Pro369= |