Canonical Allele Identifier: CA889337
Gene: PGM1 HGNC NCBI
ITGB3BP HGNC NCBI

Linked Data

dbSNP Id: rs374954710
gnomAD v2: 1-64059181-A-G
gnomAD v4: 1-63593510-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63593510A>G , CM000663.2:g.63593510A>G GRCh38
NC_000001.10:g.64059181A>G , CM000663.1:g.64059181A>G GRCh37
NC_000001.9:g.63831769A>G NCBI36
NG_016966.1:g.5235A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.8:c.22A>G (PGM1) MANE Select ENSP00000360125.3:p.Lys8Glu
ENST00000650546.1:c.22A>G (PGM1) ENSP00000497812.1:p.Lys8Glu
ENST00000371084.7:c.22A>G (PGM1) ENSP00000360125.3:p.Lys8Glu
ENST00000478138.1:n.197+15T>C (ITGB3BP)
NM_002633.2:c.22A>G (PGM1) NP_002624.2:p.Lys8Glu
NM_002633.3:c.22A>G (PGM1) MANE Select NP_002624.2:p.Lys8Glu