Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31367919C= , CM000664.2:g.31367919C= | GRCh38 |
| NC_000002.11:g.31590785C= , CM000664.1:g.31590785C= | GRCh37 |
| NC_000002.10:g.31444289C= | NCBI36 |
| NG_008871.1:g.51827G= | |
| NG_008871.2:g.51827G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379416.4:c.2197+42G= MANE Select | ENSP00000368727.3:n.2197+42G= | |
| ENST00000379416.3:c.2197+42G= | ENSP00000368727.3:n.2197+42G= | |
| NM_000379.3:c.2197+42G= | NP_000370.2:n.2197+42G= | |
| XM_011533095.1:c.2194+42G= | XP_011531397.1:n.2194+42G= | |
| XM_011533096.1:c.2197+42G= | XP_011531398.1:n.2197+42G= | |
| XM_011533095.2:c.2194+42G= | XP_011531397.1:n.2194+42G= | |
| XM_011533096.2:c.2197+42G= | XP_011531398.1:n.2197+42G= | |
| NM_000379.4:c.2197+42G= MANE Select | NP_000370.2:n.2197+42G= |