Canonical Allele Identifier: CA679277725

Gene: PYGM

Linked Data

• dbSNP Id: rs1433118649
• gnomAD v3: 11-64759624-C-T
• gnomAD v4: 11-64759624-C-T
• MyVariant Identifiers: chr11:g.64527096C>T (hg19) ; chr11:g.64759624C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64759624C>T , CM000673.2:g.64759624C>T	GRCh38
NC_000011.9:g.64527096C>T , CM000673.1:g.64527096C>T	GRCh37
NC_000011.8:g.64283672C>T	NCBI36
NG_013018.1:g.6092G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.243+32G>A MANE Select	ENSP00000164139.3:n.243+32G>A
ENST00000164139.3:c.243+32G>A	ENSP00000164139.3:n.243+32G>A
ENST00000377432.7:c.243+32G>A	ENSP00000366650.3:n.243+32G>A
NM_001164716.1:c.243+32G>A	NP_001158188.1:n.243+32G>A
NM_005609.2:c.243+32G>A	NP_005600.1:n.243+32G>A
NM_005609.3:c.243+32G>A	NP_005600.1:n.243+32G>A
NM_005609.4:c.243+32G>A MANE Select	NP_005600.1:n.243+32G>A