HGVS | Genome Assembly |
---|---|
NC_000007.14:g.19117030C>A , CM000669.2:g.19117030C>A | GRCh38 |
NC_000007.13:g.19156653C>A , CM000669.1:g.19156653C>A | GRCh37 |
NC_000007.12:g.19123178C>A | NCBI36 |
NG_008114.1:g.5643G>T | |
NG_008114.2:g.5643G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242261.6:c.292G>T MANE Select | ENSP00000242261.5:p.Gly98Trp | |
ENST00000242261.5:c.292G>T | ENSP00000242261.5:p.Gly98Trp | |
ENST00000354571.5:c.89G>T | ||
NM_000474.3:c.292G>T | NP_000465.1:p.Gly98Trp | |
XM_011515496.1:c.292G>T | XP_011513798.1:p.Gly98Trp | |
NR_149001.1:n.643G>T | ||
NM_000474.4:c.292G>T MANE Select | NP_000465.1:p.Gly98Trp | |
NR_149001.2:n.607G>T |