Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.177442422C= , CM000666.2:g.177442422C= | GRCh38 |
| NC_000004.11:g.178363576C= , CM000666.1:g.178363576C= | GRCh37 |
| NC_000004.10:g.178600570C= | NCBI36 |
| NG_011845.2:g.5082G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264595.7:c.-47G= MANE Select | ENSP00000264595.2:n.-47G= | |
| ENST00000264595.6:c.-47G= | ENSP00000264595.2:n.-47G= | |
| NM_000027.3:c.-47G= | NP_000018.2:n.-47G= | |
| NM_001171988.1:c.-47G= | NP_001165459.1:n.-47G= | |
| NR_033655.1:n.82G= | ||
| XM_006714123.2:c.-47G= | XP_006714186.1:n.-47G= | |
| XR_001741155.2:n.48G= | ||
| NM_000027.4:c.-47G= MANE Select | NP_000018.2:n.-47G= | |
| NM_001171988.2:c.-47G= | NP_001165459.1:n.-47G= | |
| NR_033655.2:n.16G= |