Canonical Allele Identifier: CA950754131
Gene: PGAM1P5 HGNC NCBI

Linked Data

dbSNP Id: rs2077782715

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.95566091T>C , CM000674.2:g.95566091T>C GRCh38
NC_000012.11:g.95959867T>C , CM000674.1:g.95959867T>C GRCh37
NC_000012.10:g.94483998T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000626376.2:n.219+14291T>C