Canonical Allele Identifier: CA889322
Gene: PGM1 HGNC NCBI
ITGB3BP HGNC NCBI

Linked Data

dbSNP Id: rs374061676
gnomAD v2: 1-64059124-G-A
gnomAD v3: 1-63593453-G-A
gnomAD v4: 1-63593453-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63593453G>A , CM000663.2:g.63593453G>A GRCh38
NC_000001.10:g.64059124G>A , CM000663.1:g.64059124G>A GRCh37
NC_000001.9:g.63831712G>A NCBI36
NG_016966.1:g.5178G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.8:c.-36G>A (PGM1) MANE Select ENSP00000360125.3:n.-36G>A
ENST00000650546.1:c.-36G>A (PGM1) ENSP00000497812.1:n.-36G>A
ENST00000371084.7:c.-36G>A (PGM1) ENSP00000360125.3:n.-36G>A
ENST00000478138.1:n.197+72C>T (ITGB3BP)
NM_002633.2:c.-36G>A (PGM1) NP_002624.2:n.-36G>A
NM_002633.3:c.-36G>A (PGM1) MANE Select NP_002624.2:n.-36G>A