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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.25543706C>G , CM000663.2:g.25543706C>G
GRCh38
NC_000001.10:g.25870197C>G , CM000663.1:g.25870197C>G
GRCh37
NC_000001.9:g.25742784C>G
NCBI36
NG_008932.1:g.5122C>G , LRG_276:g.5122C>G
Transcript Alleles
HGVS
Amino-acid Change
ENST00000374338.5:c.8C>G
MANE Select
ENSP00000363458.4:p.Ala3Gly
ENST00000374338.4:c.8C>G
ENSP00000363458.4:p.Ala3Gly
NM_015627.2:c.8C>G , LRG_276t1:c.8C>G
NP_056442.2:p.Ala3Gly
XM_006710559.2:c.8C>G
XP_006710622.1:p.Ala3Gly
XM_006710560.2:c.8C>G
XP_006710623.1:p.Ala3Gly
XM_006710561.2:c.8C>G
XP_006710624.1:p.Ala3Gly
XM_011541209.1:c.8C>G
XP_011539511.1:p.Ala3Gly
XM_011541210.1:c.8C>G
XP_011539512.1:p.Ala3Gly
XM_011541211.1:c.8C>G
XP_011539513.1:p.Ala3Gly
XM_011541212.1:c.8C>G
XP_011539514.1:p.Ala3Gly
XR_426598.2:n.127C>G
XR_946602.1:n.127C>G
XR_946603.1:n.127C>G
XM_006710559.4:c.8C>G
XP_006710622.1:p.Ala3Gly
XM_006710560.4:c.8C>G
XP_006710623.1:p.Ala3Gly
XM_006710561.4:c.8C>G
XP_006710624.1:p.Ala3Gly
XM_011541209.3:c.8C>G
XP_011539511.1:p.Ala3Gly
XM_011541210.3:c.8C>G
XP_011539512.1:p.Ala3Gly
XM_011541211.3:c.8C>G
XP_011539513.1:p.Ala3Gly
XM_011541212.3:c.8C>G
XP_011539514.1:p.Ala3Gly
XM_017000995.2:c.8C>G
XP_016856484.1:p.Ala3Gly
XR_001737112.2:n.78C>G
XR_001737113.2:n.78C>G
XR_002956258.1:n.78C>G
XR_426598.4:n.78C>G
XR_946602.3:n.78C>G
XR_946603.3:n.78C>G
NM_015627.3:c.8C>G
MANE Select
NP_056442.2:p.Ala3Gly