Canonical Allele Identifier: CA340643502

Gene: PGM1

Linked Data

• dbSNP Id: rs1648943172
• gnomAD v3: 1-63623596-T-C
• gnomAD v4: 1-63623596-T-C
• MyVariant Identifiers: chr1:g.64089267T>C (hg19) ; chr1:g.63623596T>C (hg38)

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