Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.169282951G= , CM000664.2:g.169282951G= | GRCh38 |
| NC_000002.11:g.170139461G= , CM000664.1:g.170139461G= | GRCh37 |
| NC_000002.10:g.169847707G= | NCBI36 |
| NG_012634.1:g.84662C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000649046.1:c.1093C= MANE Select | ENSP00000496870.1:p.Arg365= | |
| ENST00000263816.7:c.1093C= | ENSP00000263816.3:p.Arg365= | |
| ENST00000443831.1:c.1093C= | ENSP00000409813.1:p.Arg365= | |
| NM_004525.2:c.1093C= | NP_004516.2:p.Arg365= | |
| XM_011511183.1:c.1093C= | XP_011509485.1:p.Arg365= | |
| XM_011511185.1:c.1093C= | XP_011509487.1:p.Arg365= | |
| NM_004525.3:c.1093C= MANE Select | NP_004516.2:p.Arg365= | |
| XM_011511183.3:c.1093C= | XP_011509485.1:p.Arg365= |