HGVS | Genome Assembly |
---|---|
NC_000023.11:g.8587621T= , CM000685.2:g.8587621T= | GRCh38 |
NC_000023.10:g.8555662T= , CM000685.1:g.8555662T= | GRCh37 |
NC_000023.9:g.8515662T= | NCBI36 |
NG_007088.1:g.149566A= | |
NG_007088.2:g.149566A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262648.8:c.726+173A= MANE Select | ENSP00000262648.3:n.726+173A= | |
ENST00000262648.7:c.726+173A= | ENSP00000262648.3:n.726+173A= | |
ENST00000619786.1:c.723+173A= | ENSP00000478734.1:n.723+173A= | |
NM_000216.2:c.726+173A= | NP_000207.2:n.726+173A= | |
XM_005274501.3:c.726+173A= | XP_005274558.1:n.726+173A= | |
NM_000216.3:c.726+173A= | NP_000207.2:n.726+173A= | |
XM_005274501.4:c.726+173A= | XP_005274558.1:n.726+173A= | |
NM_000216.4:c.726+173A= MANE Select | NP_000207.2:n.726+173A= |