Canonical Allele Identifier: CA10625542
Gene: PRKAG2 HGNC NCBI
PRKAG2-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 359363
ClinVar RCV Id: RCV000320365 RCV000377271 RCV001795989
dbSNP Id: rs886062107
MyVariant Identifiers: chr7:g.151574222C>A (hg19) chr7:g.151877137C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151877137C>A , CM000669.2:g.151877137C>A GRCh38
NC_000007.13:g.151574222C>A , CM000669.1:g.151574222C>A GRCh37
NC_000007.12:g.151205155C>A NCBI36
NG_007486.1:g.5095G>T
NG_007486.2:g.5095G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000652321.2:c.-517G>T (PRKAG2) ENSP00000498886.2:n.-517G>T
NM_016203.3:c.-517G>T (PRKAG2) NP_057287.2:n.-517G>T
NR_038926.1:n.96C>A (PRKAG2-AS1)
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