Canonical Allele Identifier: CA241398391

Gene: PGAM1P5

Linked Data

• dbSNP Id: rs1000040578
• MyVariant Identifiers: chr12:g.95959624T>C (hg19) ; chr12:g.95565848T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.95565848T>C , CM000674.2:g.95565848T>C	GRCh38
NC_000012.11:g.95959624T>C , CM000674.1:g.95959624T>C	GRCh37
NC_000012.10:g.94483755T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000626376.2:n.219+14048T>C