Canonical Allele Identifier: CA23820536
Gene: PGM1 HGNC NCBI
ITGB3BP HGNC NCBI

Linked Data

dbSNP Id: rs937170258
gnomAD v2: 1-64059073-C-A
gnomAD v3: 1-63593402-C-A
gnomAD v4: 1-63593402-C-A
MyVariant Identifiers: chr1:g.64059073C>A (hg19) chr1:g.63593402C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63593402C>A , CM000663.2:g.63593402C>A GRCh38
NC_000001.10:g.64059073C>A , CM000663.1:g.64059073C>A GRCh37
NC_000001.9:g.63831661C>A NCBI36
NG_016966.1:g.5127C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.7:c.-87C>A (PGM1) ENSP00000360125.3:n.-87C>A
ENST00000478138.1:n.197+123G>T (ITGB3BP)
NM_002633.2:c.-87C>A (PGM1) NP_002624.2:n.-87C>A
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