HGVS | Genome Assembly |
---|---|
NC_000023.11:g.8731882C>G , CM000685.2:g.8731882C>G | GRCh38 |
NC_000023.10:g.8699923C>G , CM000685.1:g.8699923C>G | GRCh37 |
NC_000023.9:g.8659923C>G | NCBI36 |
NG_007088.1:g.5305G>C | |
NG_007088.2:g.5305G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262648.8:c.155G>C MANE Select | ENSP00000262648.3:p.Arg52Thr | |
ENST00000262648.7:c.155G>C | ENSP00000262648.3:p.Arg52Thr | |
ENST00000619786.1:c.152G>C | ENSP00000478734.1:p.Arg51Thr | |
NM_000216.2:c.155G>C | NP_000207.2:p.Arg52Thr | |
XM_005274501.3:c.155G>C | XP_005274558.1:p.Arg52Thr | |
NM_000216.3:c.155G>C | NP_000207.2:p.Arg52Thr | |
XM_005274501.4:c.155G>C | XP_005274558.1:p.Arg52Thr | |
NM_000216.4:c.155G>C MANE Select | NP_000207.2:p.Arg52Thr |