Canonical Allele Identifier: CA693789325

Gene: PGAM1P5

Linked Data

• dbSNP Id: rs1411185068
• gnomAD v3: 12-95565964-C-G
• gnomAD v4: 12-95565964-C-G
• MyVariant Identifiers: chr12:g.95959740C>G (hg19) ; chr12:g.95565964C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.95565964C>G , CM000674.2:g.95565964C>G	GRCh38
NC_000012.11:g.95959740C>G , CM000674.1:g.95959740C>G	GRCh37
NC_000012.10:g.94483871C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000626376.2:n.219+14164C>G