Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31339495T>A , CM000664.2:g.31339495T>A | GRCh38 |
| NC_000002.11:g.31562361T>A , CM000664.1:g.31562361T>A | GRCh37 |
| NC_000002.10:g.31415865T>A | NCBI36 |
| NG_008871.1:g.80251A>T | |
| NG_008871.2:g.80251A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000379.4:c.3768A>T MANE Select | NP_000370.2:p.Ala1256= |
| ENST00000379416.4:c.3768A>T MANE Select | ENSP00000368727.3:p.Ala1256= |
| NM_000379.3:c.3768A>T | NP_000370.2:p.Ala1256= |
| ENST00000379416.3:c.3768A>T | ENSP00000368727.3:p.Ala1256= |
| XM_011533095.1:c.3765A>T | XP_011531397.1:p.Ala1255= |
| XM_011533095.2:c.3765A>T | XP_011531397.1:p.Ala1255= |