Canonical Allele Identifier: CA693789329

Gene: PGAM1P5

Linked Data

• dbSNP Id: rs1244545336
• gnomAD v3: 12-95565979-T-A
• gnomAD v4: 12-95565979-T-A
• MyVariant Identifiers: chr12:g.95959755T>A (hg19) ; chr12:g.95565979T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.95565979T>A , CM000674.2:g.95565979T>A	GRCh38
NC_000012.11:g.95959755T>A , CM000674.1:g.95959755T>A	GRCh37
NC_000012.10:g.94483886T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000626376.2:n.219+14179T>A