Canonical Allele Identifier: CA693789338
Gene: PGAM1P5 HGNC NCBI

Linked Data

dbSNP Id: rs1269133216
MyVariant Identifiers: chr12:g.95959786C>A (hg19) chr12:g.95566010C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.95566010C>A , CM000674.2:g.95566010C>A GRCh38
NC_000012.11:g.95959786C>A , CM000674.1:g.95959786C>A GRCh37
NC_000012.10:g.94483917C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000626376.2:n.219+14210C>A
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Search 100 bp 3'