Canonical Allele Identifier: CA340638974
Gene: PGM1 HGNC NCBI
ITGB3BP HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.64059214A>C (hg19) chr1:g.63593543A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63593543A>C , CM000663.2:g.63593543A>C GRCh38
NC_000001.10:g.64059214A>C , CM000663.1:g.64059214A>C GRCh37
NC_000001.9:g.63831802A>C NCBI36
NG_016966.1:g.5268A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.8:c.55A>C (PGM1) MANE Select ENSP00000360125.3:p.Thr19Pro
ENST00000650546.1:c.55A>C (PGM1) ENSP00000497812.1:p.Thr19Pro
ENST00000371084.7:c.55A>C (PGM1) ENSP00000360125.3:p.Thr19Pro
ENST00000478138.1:n.179T>G (ITGB3BP)
NM_002633.2:c.55A>C (PGM1) NP_002624.2:p.Thr19Pro
NM_002633.3:c.55A>C (PGM1) MANE Select NP_002624.2:p.Thr19Pro
Search 100 bp 5'
Search 100 bp 3'