Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.85589292T= , CM000664.2:g.85589292T= | GRCh38 |
| NC_000002.11:g.85816415T= , CM000664.1:g.85816415T= | GRCh37 |
| NC_000002.10:g.85669926T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306384.5:c.4-2433T= MANE Select | ENSP00000305647.4:n.4-2433T= | |
| ENST00000306384.4:c.4-2433T= | ENSP00000305647.4:n.4-2433T= | |
| NM_006634.2:c.4-2433T= | NP_006625.1:n.4-2433T= | |
| NM_006634.3:c.4-2433T= MANE Select | NP_006625.1:n.4-2433T= |