Canonical Allele Identifier: CA2614192136
Gene: PYGM HGNC NCBI

Linked Data

gnomAD v4: 11-64759971-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759971G>T , CM000673.2:g.64759971G>T GRCh38
NC_000011.9:g.64527443G>T , CM000673.1:g.64527443G>T GRCh37
NC_000011.8:g.64284019G>T NCBI36
NG_013018.1:g.5745C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.-73C>A MANE Select ENSP00000164139.3:n.-73C>A
ENST00000164139.3:c.-73C>A ENSP00000164139.3:n.-73C>A
ENST00000377432.7:c.-73C>A ENSP00000366650.3:n.-73C>A
NM_001164716.1:c.-73C>A NP_001158188.1:n.-73C>A
NM_005609.2:c.-73C>A NP_005600.1:n.-73C>A
NM_005609.3:c.-73C>A NP_005600.1:n.-73C>A
NM_005609.4:c.-73C>A MANE Select NP_005600.1:n.-73C>A
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