Canonical Allele Identifier: CA837264682
Gene: GNA12 HGNC NCBI

Linked Data

dbSNP Id: rs1414626233
MyVariant Identifiers: chr7:g.2870002G>A (hg19) chr7:g.2830368G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.2830368G>A , CM000669.2:g.2830368G>A GRCh38
NC_000007.13:g.2870002G>A , CM000669.1:g.2870002G>A GRCh37
NC_000007.12:g.2836528G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000275364.8:c.309+13485C>T MANE Select ENSP00000275364.3:n.309+13485C>T
ENST00000275364.7:c.309+13485C>T ENSP00000275364.3:n.309+13485C>T
NM_001293092.1:c.309+13485C>T NP_001280021.1:n.309+13485C>T
NM_007353.2:c.309+13485C>T NP_031379.2:n.309+13485C>T
XM_011515288.1:c.19-35225C>T XP_011513590.1:n.19-35225C>T
XM_011515288.3:c.19-35225C>T XP_011513590.1:n.19-35225C>T
NM_007353.3:c.309+13485C>T MANE Select NP_031379.2:n.309+13485C>T
NM_001293092.2:c.309+13485C>T NP_001280021.1:n.309+13485C>T
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