HGVS | Genome Assembly |
---|---|
NC_000007.14:g.19116740C>A , CM000669.2:g.19116740C>A | GRCh38 |
NC_000007.13:g.19156363C>A , CM000669.1:g.19156363C>A | GRCh37 |
NC_000007.12:g.19122888C>A | NCBI36 |
NG_008114.1:g.5933G>T | |
NG_008114.2:g.5933G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242261.6:c.582G>T MANE Select | ENSP00000242261.5:p.Gly194= | |
ENST00000242261.5:c.582G>T | ENSP00000242261.5:p.Gly194= | |
ENST00000354571.5:c.379G>T | ||
ENST00000443687.5:c.185G>T | ||
NM_000474.3:c.582G>T | NP_000465.1:p.Gly194= | |
XM_011515496.1:c.582G>T | XP_011513798.1:p.Gly194= | |
NR_149001.1:n.933G>T | ||
NM_000474.4:c.582G>T MANE Select | NP_000465.1:p.Gly194= | |
NR_149001.2:n.897G>T |