Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52023975G>A , CM000666.2:g.52023975G>A | GRCh38 |
| NC_000004.11:g.52890141G>A , CM000666.1:g.52890141G>A | GRCh37 |
| NC_000004.10:g.52584898G>A | NCBI36 |
| NG_008891.1:g.19345C>T , LRG_204:g.19345C>T | |
| NG_053164.1:g.1337C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000232.5:c.939C>T MANE Select | NP_000223.1:p.Pro313= |
| ENST00000381431.10:c.939C>T MANE Select | ENSP00000370839.6:p.Pro313= |
| NM_000232.4:c.939C>T , LRG_204t1:c.939C>T | NP_000223.1:p.Pro313= |
| ENST00000381431.9:c.939C>T | ENSP00000370839.5:p.Pro313= |
| XM_006714049.2:c.642C>T | XP_006714112.1:p.Pro214= |
| XM_011534403.1:c.729C>T | XP_011532705.1:p.Pro243= |
| XM_011534404.1:c.642C>T | XP_011532706.1:p.Pro214= |