Canonical Allele Identifier: CA1683354002

Gene: GNA12

Linked Data

• dbSNP Id: rs1793577051

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2830377C>G , CM000669.2:g.2830377C>G	GRCh38
NC_000007.13:g.2870011C>G , CM000669.1:g.2870011C>G	GRCh37
NC_000007.12:g.2836537C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000275364.8:c.309+13476G>C MANE Select	ENSP00000275364.3:n.309+13476G>C
ENST00000275364.7:c.309+13476G>C	ENSP00000275364.3:n.309+13476G>C
NM_001293092.1:c.309+13476G>C	NP_001280021.1:n.309+13476G>C
NM_007353.2:c.309+13476G>C	NP_031379.2:n.309+13476G>C
XM_011515288.1:c.19-35234G>C	XP_011513590.1:n.19-35234G>C
XM_011515288.3:c.19-35234G>C	XP_011513590.1:n.19-35234G>C
NM_007353.3:c.309+13476G>C MANE Select	NP_031379.2:n.309+13476G>C
NM_001293092.2:c.309+13476G>C	NP_001280021.1:n.309+13476G>C