Canonical Allele Identifier: CA340643502
Gene: PGM1 HGNC NCBI

Linked Data

dbSNP Id: rs1648943172
gnomAD v3: 1-63623596-T-C
gnomAD v4: 1-63623596-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63623596T>C , CM000663.2:g.63623596T>C GRCh38
NC_000001.10:g.64089267T>C , CM000663.1:g.64089267T>C GRCh37
NC_000001.9:g.63861855T>C NCBI36
NG_016966.1:g.35321T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371084.8:c.247-5829T>C MANE Select ENSP00000360125.3:n.247-5829T>C
ENST00000650546.1:c.247-5829T>C ENSP00000497812.1:n.247-5829T>C
ENST00000371083.4:c.136T>C ENSP00000360124.4:p.Tyr46His
ENST00000371084.7:c.247-5829T>C ENSP00000360125.3:n.247-5829T>C
ENST00000540265.5:c.-345-5829T>C ENSP00000443449.1:n.-345-5829T>C
NM_001172818.1:c.136T>C NP_001166289.1:p.Tyr46His
NM_001172819.1:c.-345-5829T>C NP_001166290.1:n.-345-5829T>C
NM_002633.2:c.247-5829T>C NP_002624.2:n.247-5829T>C
NM_002633.3:c.247-5829T>C MANE Select NP_002624.2:n.247-5829T>C
NM_001172819.2:c.-345-5829T>C NP_001166290.1:n.-345-5829T>C