Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.45529095C>T , CM000681.2:g.45529095C>T | GRCh38 |
| NC_000019.9:g.46032353C>T , CM000681.1:g.46032353C>T | GRCh37 |
| NC_000019.8:g.50724193C>T | NCBI36 |
| NG_013332.1:g.60770G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001017989.2:c.504G>A | NP_001017989.2:p.Pro168= |
| NM_001017989.3:c.504G>A | NP_001017989.2:p.Pro168= |
| ENST00000323060.3:c.504G>A | ENSP00000319817.3:p.Pro168= |
| ENST00000323060.4:c.504G>A | ENSP00000319817.3:p.Pro168= |
| XM_011527348.1:c.345G>A | XP_011525650.1:p.Pro115= |