HGVS | Genome Assembly |
---|---|
NC_000006.12:g.33080786G= , CM000668.2:g.33080786G= | GRCh38 |
NC_000006.11:g.33048563G= , CM000668.1:g.33048563G= | GRCh37 |
NC_000006.10:g.33156541G= | NCBI36 |
NG_033241.1:g.4993C= | |
NG_033242.1:g.9861G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000418931.7:c.215G= MANE Select | ENSP00000408146.2:p.Gly72= | |
ENST00000416804.1:c.115G= | ||
ENST00000418931.6:c.215G= | ENSP00000408146.2:p.Gly72= | |
ENST00000428835.5:c.146G= | ENSP00000412654.1:p.Gly49= | |
ENST00000469120.1:n.247G= | ||
ENST00000471184.5:n.264G= | ||
ENST00000488575.1:n.264G= | ||
ENST00000498038.1:n.344G= | ||
NM_002121.5:c.215G= | NP_002112.3:p.Gly72= | |
XM_006715078.2:c.-98G= | XP_006715141.1:n.-98G= | |
NM_002121.6:c.215G= MANE Select | NP_002112.3:p.Gly72= |