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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.155294679C>A , CM000663.2:g.155294679C>A
GRCh38
NC_000001.10:g.155264470C>A , CM000663.1:g.155264470C>A
GRCh37
NC_000001.9:g.153531094C>A
NCBI36
NG_011677.1:g.11756G>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000342741.6:c.768G>T
MANE Select
ENSP00000339933.4:p.Gly256=
ENST00000342741.4:c.768G>T
ENSP00000339933.4:p.Gly256=
ENST00000392414.7:c.675G>T
ENSP00000376214.3:p.Gly225=
NM_000298.5:c.768G>T
NP_000289.1:p.Gly256=
NM_181871.3:c.675G>T
NP_870986.1:p.Gly225=
XM_005245266.3:c.927G>T
XP_005245323.1:p.Gly309=
XM_006711386.2:c.576G>T
XP_006711449.1:p.Gly192=
XM_011509639.1:c.927G>T
XP_011507941.1:p.Gly309=
XM_011509640.1:c.576G>T
XP_011507942.1:p.Gly192=
NM_000298.6:c.768G>T
MANE Select
NP_000289.1:p.Gly256=
XM_006711386.4:c.576G>T
XP_006711449.1:p.Gly192=
XM_011509640.3:c.576G>T
XP_011507942.1:p.Gly192=
XM_017001493.1:c.768G>T
XP_016856982.1:p.Gly256=
NM_181871.4:c.675G>T
NP_870986.1:p.Gly225=