HGVS | Genome Assembly |
---|---|
NC_000001.11:g.147908292G>T , CM000663.2:g.147908292G>T | GRCh38 |
NC_000001.10:g.147380419G>T , CM000663.1:g.147380419G>T | GRCh37 |
NC_000001.9:g.145847043G>T | NCBI36 |
NG_016242.1:g.10474G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369235.2:c.337G>T MANE Select | ENSP00000358238.1:p.Glu113Ter | |
ENST00000369235.1:c.337G>T | ENSP00000358238.1:p.Glu113Ter | |
NM_005267.4:c.337G>T | NP_005258.2:p.Glu113Ter | |
XM_011509416.1:c.337G>T | XP_011507718.1:p.Glu113Ter | |
XM_011509417.1:c.337G>T | XP_011507719.1:p.Glu113Ter | |
XM_011509417.2:c.337G>T | XP_011507719.1:p.Glu113Ter | |
XR_002956281.1:n.1252G>T | ||
NM_005267.5:c.337G>T MANE Select | NP_005258.2:p.Glu113Ter |