HGVS | Genome Assembly |
---|---|
NC_000023.11:g.8731897G>A , CM000685.2:g.8731897G>A | GRCh38 |
NC_000023.10:g.8699938G>A , CM000685.1:g.8699938G>A | GRCh37 |
NC_000023.9:g.8659938G>A | NCBI36 |
NG_007088.1:g.5290C>T | |
NG_007088.2:g.5290C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000262648.8:c.140C>T MANE Select | ENSP00000262648.3:p.Ala47Val | |
ENST00000262648.7:c.140C>T | ENSP00000262648.3:p.Ala47Val | |
ENST00000619786.1:c.138C>T | ENSP00000478734.1:p.Arg46= | |
NM_000216.2:c.140C>T | NP_000207.2:p.Ala47Val | |
XM_005274501.3:c.140C>T | XP_005274558.1:p.Ala47Val | |
NM_000216.3:c.140C>T | NP_000207.2:p.Ala47Val | |
XM_005274501.4:c.140C>T | XP_005274558.1:p.Ala47Val | |
NM_000216.4:c.140C>T MANE Select | NP_000207.2:p.Ala47Val |