Canonical Allele Identifier: CA1683353990
Gene: GNA12 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.2830353G= , CM000669.2:g.2830353G= GRCh38
NC_000007.13:g.2869987G= , CM000669.1:g.2869987G= GRCh37
NC_000007.12:g.2836513G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000275364.8:c.309+13500C= MANE Select ENSP00000275364.3:n.309+13500C=
ENST00000275364.7:c.309+13500C= ENSP00000275364.3:n.309+13500C=
NM_001293092.1:c.309+13500C= NP_001280021.1:n.309+13500C=
NM_007353.2:c.309+13500C= NP_031379.2:n.309+13500C=
XM_011515288.1:c.19-35210C= XP_011513590.1:n.19-35210C=
XM_011515288.3:c.19-35210C= XP_011513590.1:n.19-35210C=
NM_007353.3:c.309+13500C= MANE Select NP_031379.2:n.309+13500C=
NM_001293092.2:c.309+13500C= NP_001280021.1:n.309+13500C=
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