Canonical Allele Identifier: CA889494
Gene: PGM1 HGNC NCBI

Linked Data

dbSNP Id: rs775543045
gnomAD v2: 1-64095099-G-A
gnomAD v4: 1-63629428-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63629428G>A , CM000663.2:g.63629428G>A GRCh38
NC_000001.10:g.64095099G>A , CM000663.1:g.64095099G>A GRCh37
NC_000001.9:g.63867687G>A NCBI36
NG_016966.1:g.41153G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371084.8:c.250G>A MANE Select ENSP00000360125.3:p.Gly84Ser
ENST00000650546.1:c.250G>A ENSP00000497812.1:p.Gly84Ser
ENST00000371083.4:c.304G>A ENSP00000360124.4:p.Gly102Ser
ENST00000371084.7:c.250G>A ENSP00000360125.3:p.Gly84Ser
ENST00000540265.5:c.-342G>A ENSP00000443449.1:n.-342G>A
NM_001172818.1:c.304G>A NP_001166289.1:p.Gly102Ser
NM_001172819.1:c.-342G>A NP_001166290.1:n.-342G>A
NM_002633.2:c.250G>A NP_002624.2:p.Gly84Ser
NM_002633.3:c.250G>A MANE Select NP_002624.2:p.Gly84Ser
NM_001172819.2:c.-342G>A NP_001166290.1:n.-342G>A