Canonical Allele Identifier: CA474958958
Gene: PYGM HGNC NCBI

Linked Data

ClinVar Variation Id: 1535676
ClinVar RCV Id: RCV002072741
dbSNP Id: rs1392210978
gnomAD v2: 11-64519105-C-T
gnomAD v4: 11-64751633-C-T
MyVariant Identifiers: chr11:g.64519105C>T (hg19) chr11:g.64751633C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64751633C>T , CM000673.2:g.64751633C>T GRCh38
NC_000011.9:g.64519105C>T , CM000673.1:g.64519105C>T GRCh37
NC_000011.8:g.64275681C>T NCBI36
NG_013018.1:g.14083G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.1791G>A MANE Select ENSP00000164139.3:p.Lys597=
ENST00000164139.3:c.1791G>A ENSP00000164139.3:p.Lys597=
ENST00000377432.7:c.1527G>A ENSP00000366650.3:p.Lys509=
ENST00000462303.1:n.115G>A
NM_001164716.1:c.1527G>A NP_001158188.1:p.Lys509=
NM_005609.2:c.1791G>A NP_005600.1:p.Lys597=
NM_005609.3:c.1791G>A NP_005600.1:p.Lys597=
NM_005609.4:c.1791G>A MANE Select NP_005600.1:p.Lys597=
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