Canonical Allele Identifier: CA1171556355
Gene: PGM1 HGNC NCBI
ITGB3BP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63593585G= , CM000663.2:g.63593585G= GRCh38
NC_000001.10:g.64059256G= , CM000663.1:g.64059256G= GRCh37
NC_000001.9:g.63831844G= NCBI36
NG_016966.1:g.5310G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.8:c.97G= (PGM1) MANE Select ENSP00000360125.3:p.Ala33=
ENST00000650546.1:c.97G= (PGM1) ENSP00000497812.1:p.Ala33=
ENST00000371084.7:c.97G= (PGM1) ENSP00000360125.3:p.Ala33=
ENST00000478138.1:n.137C= (ITGB3BP)
NM_002633.2:c.97G= (PGM1) NP_002624.2:p.Ala33=
NM_002633.3:c.97G= (PGM1) MANE Select NP_002624.2:p.Ala33=