Canonical Allele Identifier: CA693789386
Gene: PGAM1P5 HGNC NCBI

Linked Data

dbSNP Id: rs1249532736
MyVariant Identifiers: chr12:g.95959868A>G (hg19) chr12:g.95566092A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.95566092A>G , CM000674.2:g.95566092A>G GRCh38
NC_000012.11:g.95959868A>G , CM000674.1:g.95959868A>G GRCh37
NC_000012.10:g.94483999A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000626376.2:n.219+14292A>G
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