Canonical Allele Identifier: CA693789229

Gene: PGAM1P5

Linked Data

• dbSNP Id: rs1309180807
• gnomAD v3: 12-95565844-A-G
• gnomAD v4: 12-95565844-A-G
• MyVariant Identifiers: chr12:g.95959620A>G (hg19) ; chr12:g.95565844A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.95565844A>G , CM000674.2:g.95565844A>G	GRCh38
NC_000012.11:g.95959620A>G , CM000674.1:g.95959620A>G	GRCh37
NC_000012.10:g.94483751A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000626376.2:n.219+14044A>G