Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.39543931C= , CM000675.2:g.39543931C= | GRCh38 |
| NC_000013.10:g.40118068C= , CM000675.1:g.40118068C= | GRCh37 |
| NC_000013.9:g.39016068C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005780.3:c.385+56901G= MANE Select | NP_005771.1:n.385+56901G= |
| ENST00000379589.4:c.385+56901G= MANE Select | ENSP00000368908.3:n.385+56901G= |
| NM_005780.2:c.385+56901G= | NP_005771.1:n.385+56901G= |
| ENST00000379589.3:c.385+56901G= | ENSP00000368908.3:n.385+56901G= |
| ENST00000648377.1:c.385+56901G= | ENSP00000496801.1:n.385+56901G= |
| XM_011534861.1:c.385+56901G= | XP_011533163.1:n.385+56901G= |