HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240869242G>T , CM000664.2:g.240869242G>T | GRCh38 |
NC_000002.11:g.241808659G>T , CM000664.1:g.241808659G>T | GRCh37 |
NC_000002.10:g.241457332G>T | NCBI36 |
NG_008005.1:g.5498G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000307503.4:c.238G>T MANE Select | ENSP00000302620.3:p.Gly80Cys | |
ENST00000307503.3:c.238G>T | ENSP00000302620.3:p.Gly80Cys | |
ENST00000472436.1:n.258G>T | ||
NM_000030.2:c.238G>T | NP_000021.1:p.Gly80Cys | |
XR_924060.1:n.405+991C>A | ||
NM_000030.3:c.238G>T MANE Select | NP_000021.1:p.Gly80Cys |