HGVS | Genome Assembly |
---|---|
NC_000013.11:g.33054015G= , CM000675.2:g.33054015G= | GRCh38 |
NC_000013.10:g.33628152G= , CM000675.1:g.33628152G= | GRCh37 |
NC_000013.9:g.32526152G= | NCBI36 |
NG_011485.1:g.42582G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000380099.4:c.1068G= MANE Select | ENSP00000369442.3:p.Glu356= | |
ENST00000380099.3:c.1068G= | ENSP00000369442.3:p.Glu356= | |
ENST00000487852.1:n.1076G= | ||
NM_004795.3:c.1068G= | NP_004786.2:p.Glu356= | |
XM_006719895.1:c.147G= | XP_006719958.1:p.Glu49= | |
XM_006719895.2:c.147G= | XP_006719958.1:p.Glu49= | |
NM_004795.4:c.1068G= MANE Select | NP_004786.2:p.Glu356= |