Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.135789640C>T , CM000664.2:g.135789640C>T | GRCh38 |
| NC_000002.11:g.136547210C>T , CM000664.1:g.136547210C>T | GRCh37 |
| NC_000002.10:g.136263680C>T | NCBI36 |
| NG_008104.2:g.70530G>A , LRG_338:g.70530G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264162.7:c.5494G>A MANE Select | ENSP00000264162.2:p.Ala1832Thr | |
| ENST00000264162.6:c.5494G>A | ENSP00000264162.2:p.Ala1832Thr | |
| NM_002299.2:c.5494G>A , LRG_338t1:c.5494G>A | NP_002290.2:p.Ala1832Thr | |
| NM_002299.3:c.5494G>A | NP_002290.2:p.Ala1832Thr | |
| NM_002299.4:c.5494G>A MANE Select | NP_002290.2:p.Ala1832Thr |