Canonical Allele Identifier: CA1683353995
Gene: GNA12 HGNC NCBI

Linked Data

dbSNP Id: rs1793576798
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.2830367G>C , CM000669.2:g.2830367G>C GRCh38
NC_000007.13:g.2870001G>C , CM000669.1:g.2870001G>C GRCh37
NC_000007.12:g.2836527G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000275364.8:c.309+13486C>G MANE Select ENSP00000275364.3:n.309+13486C>G
ENST00000275364.7:c.309+13486C>G ENSP00000275364.3:n.309+13486C>G
NM_001293092.1:c.309+13486C>G NP_001280021.1:n.309+13486C>G
NM_007353.2:c.309+13486C>G NP_031379.2:n.309+13486C>G
XM_011515288.1:c.19-35224C>G XP_011513590.1:n.19-35224C>G
XM_011515288.3:c.19-35224C>G XP_011513590.1:n.19-35224C>G
NM_007353.3:c.309+13486C>G MANE Select NP_031379.2:n.309+13486C>G
NM_001293092.2:c.309+13486C>G NP_001280021.1:n.309+13486C>G
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