Canonical Allele Identifier: CA418268544
Gene: PGM1 HGNC NCBI
ITGB3BP HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.64059180T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63593509T>G , CM000663.2:g.63593509T>G GRCh38
NC_000001.10:g.64059180T>G , CM000663.1:g.64059180T>G GRCh37
NC_000001.9:g.63831768T>G NCBI36
NG_016966.1:g.5234T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.8:c.21T>G (PGM1) MANE Select ENSP00000360125.3:p.Val7=
ENST00000650546.1:c.21T>G (PGM1) ENSP00000497812.1:p.Val7=
ENST00000371084.7:c.21T>G (PGM1) ENSP00000360125.3:p.Val7=
ENST00000478138.1:n.197+16A>C (ITGB3BP)
NM_002633.2:c.21T>G (PGM1) NP_002624.2:p.Val7=
NM_002633.3:c.21T>G (PGM1) MANE Select NP_002624.2:p.Val7=
Search 100 bp 5'
Search 100 bp 3'