Canonical Allele Identifier: CA6079895
Gene: PYGM HGNC NCBI

Linked Data

dbSNP Id: rs760281187
ExAC: 11:64521022 G / A
gnomAD v2: 11-64521022-G-A
gnomAD v3: 11-64753550-G-A
gnomAD v4: 11-64753550-G-A
MyVariant Identifiers: chr11:g.64521022G>A (hg19) chr11:g.64753550G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64753550G>A , CM000673.2:g.64753550G>A GRCh38
NC_000011.9:g.64521022G>A , CM000673.1:g.64521022G>A GRCh37
NC_000011.8:g.64277598G>A NCBI36
NG_013018.1:g.12166C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.1372C>T MANE Select ENSP00000164139.3:p.Arg458Cys
ENST00000164139.3:c.1372C>T ENSP00000164139.3:p.Arg458Cys
ENST00000377432.7:c.1108C>T ENSP00000366650.3:p.Arg370Cys
NM_001164716.1:c.1108C>T NP_001158188.1:p.Arg370Cys
NM_005609.2:c.1372C>T NP_005600.1:p.Arg458Cys
NM_005609.3:c.1372C>T NP_005600.1:p.Arg458Cys
NM_005609.4:c.1372C>T MANE Select NP_005600.1:p.Arg458Cys
Search 100 bp 5'
Search 100 bp 3'