Canonical Allele Identifier: CA223889549
Gene: PYGM HGNC NCBI

Linked Data

dbSNP Id: rs1006818514
gnomAD v2: 11-64527444-A-T
gnomAD v3: 11-64759972-A-T
gnomAD v4: 11-64759972-A-T
MyVariant Identifiers: chr11:g.64527444A>T (hg19) chr11:g.64759972A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759972A>T , CM000673.2:g.64759972A>T GRCh38
NC_000011.9:g.64527444A>T , CM000673.1:g.64527444A>T GRCh37
NC_000011.8:g.64284020A>T NCBI36
NG_013018.1:g.5744T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.-74T>A MANE Select ENSP00000164139.3:n.-74T>A
ENST00000164139.3:c.-74T>A ENSP00000164139.3:n.-74T>A
ENST00000377432.7:c.-74T>A ENSP00000366650.3:n.-74T>A
NM_001164716.1:c.-74T>A NP_001158188.1:n.-74T>A
NM_005609.2:c.-74T>A NP_005600.1:n.-74T>A
NM_005609.3:c.-74T>A NP_005600.1:n.-74T>A
NM_005609.4:c.-74T>A MANE Select NP_005600.1:n.-74T>A
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