Canonical Allele Identifier: CA1171556292
Gene: PGM1 HGNC NCBI
ITGB3BP HGNC NCBI

Linked Data

dbSNP Id: rs756324880
gnomAD v4: 1-63593454-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63593454T>G , CM000663.2:g.63593454T>G GRCh38
NC_000001.10:g.64059125T>G , CM000663.1:g.64059125T>G GRCh37
NC_000001.9:g.63831713T>G NCBI36
NG_016966.1:g.5179T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.8:c.-35T>G (PGM1) MANE Select ENSP00000360125.3:n.-35T>G
ENST00000650546.1:c.-35T>G (PGM1) ENSP00000497812.1:n.-35T>G
ENST00000371084.7:c.-35T>G (PGM1) ENSP00000360125.3:n.-35T>G
ENST00000478138.1:n.197+71A>C (ITGB3BP)
NM_002633.2:c.-35T>G (PGM1) NP_002624.2:n.-35T>G
NM_002633.3:c.-35T>G (PGM1) MANE Select NP_002624.2:n.-35T>G