Canonical Allele Identifier: CA474958878
Gene: PYGM HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.64518852A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64751380A>G , CM000673.2:g.64751380A>G GRCh38
NC_000011.9:g.64518852A>G , CM000673.1:g.64518852A>G GRCh37
NC_000011.8:g.64275428A>G NCBI36
NG_013018.1:g.14336T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.1914T>C MANE Select ENSP00000164139.3:p.Gly638=
ENST00000164139.3:c.1914T>C ENSP00000164139.3:p.Gly638=
ENST00000377432.7:c.1650T>C ENSP00000366650.3:p.Gly550=
ENST00000462303.1:n.238T>C
NM_001164716.1:c.1650T>C NP_001158188.1:p.Gly550=
NM_005609.2:c.1914T>C NP_005600.1:p.Gly638=
NM_005609.3:c.1914T>C NP_005600.1:p.Gly638=
NM_005609.4:c.1914T>C MANE Select NP_005600.1:p.Gly638=
Search 100 bp 5'
Search 100 bp 3'