Canonical Allele Identifier: CA474958905
Gene: PYGM HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.64518891T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64751419T>G , CM000673.2:g.64751419T>G GRCh38
NC_000011.9:g.64518891T>G , CM000673.1:g.64518891T>G GRCh37
NC_000011.8:g.64275467T>G NCBI36
NG_013018.1:g.14297A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.1875A>C MANE Select ENSP00000164139.3:p.Thr625=
ENST00000164139.3:c.1875A>C ENSP00000164139.3:p.Thr625=
ENST00000377432.7:c.1611A>C ENSP00000366650.3:p.Thr537=
ENST00000462303.1:n.199A>C
NM_001164716.1:c.1611A>C NP_001158188.1:p.Thr537=
NM_005609.2:c.1875A>C NP_005600.1:p.Thr625=
NM_005609.3:c.1875A>C NP_005600.1:p.Thr625=
NM_005609.4:c.1875A>C MANE Select NP_005600.1:p.Thr625=
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