Canonical Allele Identifier: CA241398489
Gene: PGAM1P5 HGNC NCBI

Linked Data

dbSNP Id: rs920478462
MyVariant Identifiers: chr12:g.95959772C>T (hg19) chr12:g.95565996C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.95565996C>T , CM000674.2:g.95565996C>T GRCh38
NC_000012.11:g.95959772C>T , CM000674.1:g.95959772C>T GRCh37
NC_000012.10:g.94483903C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000626376.2:n.219+14196C>T
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