Canonical Allele Identifier: CA241398450
Gene: PGAM1P5 HGNC NCBI

Linked Data

dbSNP Id: rs960777129
gnomAD v2: 12-95959698-A-G
gnomAD v3: 12-95565922-A-G
gnomAD v4: 12-95565922-A-G
MyVariant Identifiers: chr12:g.95959698A>G (hg19) chr12:g.95565922A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.95565922A>G , CM000674.2:g.95565922A>G GRCh38
NC_000012.11:g.95959698A>G , CM000674.1:g.95959698A>G GRCh37
NC_000012.10:g.94483829A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000626376.2:n.219+14122A>G
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