Canonical Allele Identifier: CA241398575
Gene: PGAM1P5 HGNC NCBI

Linked Data

dbSNP Id: rs1043993062
MyVariant Identifiers: chr12:g.95566136T>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.95566136T>G , CM000674.2:g.95566136T>G GRCh38
NC_000012.11:g.95959912T>G , CM000674.1:g.95959912T>G GRCh37
NC_000012.10:g.94484043T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000626376.2:n.219+14336T>G