Canonical Allele Identifier: CA13693679
Gene: PGAM1P5 HGNC NCBI

Linked Data

dbSNP Id: rs17356907 rs2136717865 rs2136717868 rs2136717870 rs2136717878
gnomAD v2: 12-96027759-A-G
gnomAD v3: 12-95633983-A-G
gnomAD v4: 12-95633983-A-G
MyVariant Identifiers: chr12:g.96027759A>G (hg19) chr12:g.95633983A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.95633983A>G , CM000674.2:g.95633983A>G GRCh38
NC_000012.11:g.96027759A>G , CM000674.1:g.96027759A>G GRCh37
NC_000012.10:g.94551890A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000626376.2:n.220-31700A>G
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