HGVS | Genome Assembly |
---|---|
NC_000002.12:g.85589291A= , CM000664.2:g.85589291A= | GRCh38 |
NC_000002.11:g.85816414A= , CM000664.1:g.85816414A= | GRCh37 |
NC_000002.10:g.85669925A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000306384.5:c.4-2434A= MANE Select | ENSP00000305647.4:n.4-2434A= | |
ENST00000306384.4:c.4-2434A= | ENSP00000305647.4:n.4-2434A= | |
NM_006634.2:c.4-2434A= | NP_006625.1:n.4-2434A= | |
NM_006634.3:c.4-2434A= MANE Select | NP_006625.1:n.4-2434A= |