Canonical Allele Identifier: CA23820561
Gene: PGM1 HGNC NCBI
ITGB3BP HGNC NCBI

Linked Data

dbSNP Id: rs547294819
gnomAD v3: 1-63593436-G-T
gnomAD v4: 1-63593436-G-T
MyVariant Identifiers: chr1:g.64059107G>T (hg19) chr1:g.63593436G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63593436G>T , CM000663.2:g.63593436G>T GRCh38
NC_000001.10:g.64059107G>T , CM000663.1:g.64059107G>T GRCh37
NC_000001.9:g.63831695G>T NCBI36
NG_016966.1:g.5161G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.8:c.-53G>T (PGM1) MANE Select ENSP00000360125.3:n.-53G>T
ENST00000650546.1:c.-53G>T (PGM1) ENSP00000497812.1:n.-53G>T
ENST00000371084.7:c.-53G>T (PGM1) ENSP00000360125.3:n.-53G>T
ENST00000478138.1:n.197+89C>A (ITGB3BP)
NM_002633.2:c.-53G>T (PGM1) NP_002624.2:n.-53G>T
NM_002633.3:c.-53G>T (PGM1) MANE Select NP_002624.2:n.-53G>T
Search 100 bp 5'
Search 100 bp 3'