Canonical Allele Identifier: CA152688210

Gene: GNA12

Linked Data

• dbSNP Id: rs990510528
• MyVariant Identifiers: chr7:g.2870008T>C (hg19) ; chr7:g.2830374T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2830374T>C , CM000669.2:g.2830374T>C	GRCh38
NC_000007.13:g.2870008T>C , CM000669.1:g.2870008T>C	GRCh37
NC_000007.12:g.2836534T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000275364.8:c.309+13479A>G MANE Select	ENSP00000275364.3:n.309+13479A>G
ENST00000275364.7:c.309+13479A>G	ENSP00000275364.3:n.309+13479A>G
NM_001293092.1:c.309+13479A>G	NP_001280021.1:n.309+13479A>G
NM_007353.2:c.309+13479A>G	NP_031379.2:n.309+13479A>G
XM_011515288.1:c.19-35231A>G	XP_011513590.1:n.19-35231A>G
XM_011515288.3:c.19-35231A>G	XP_011513590.1:n.19-35231A>G
NM_007353.3:c.309+13479A>G MANE Select	NP_031379.2:n.309+13479A>G
NM_001293092.2:c.309+13479A>G	NP_001280021.1:n.309+13479A>G