Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.88008234A>C , CM000666.2:g.88008234A>C | GRCh38 |
| NC_000004.11:g.88929386A>C , CM000666.1:g.88929386A>C | GRCh37 |
| NC_000004.10:g.89148410A>C | NCBI36 |
| NG_008604.1:g.5567A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000237596.7:c.501A>C MANE Select | ENSP00000237596.2:p.Pro167= | |
| ENST00000237596.6:c.501A>C | ENSP00000237596.2:p.Pro167= | |
| ENST00000506727.1:n.3A>C | ||
| NM_000297.3:c.501A>C | NP_000288.1:p.Pro167= | |
| XM_011532028.1:c.501A>C | XP_011530330.1:p.Pro167= | |
| XR_244632.2:n.596A>C | ||
| NR_156488.1:n.588A>C | ||
| XM_011532028.2:c.501A>C | XP_011530330.1:p.Pro167= | |
| NM_000297.4:c.501A>C MANE Select | NP_000288.1:p.Pro167= | |
| NR_156488.2:n.600A>C |