Canonical Allele Identifier: CA2614192158
Gene: PYGM HGNC NCBI

Linked Data

gnomAD v4: 11-64759992-AG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759996del , CM000673.2:g.64759996del GRCh38
NC_000011.9:g.64527468del , CM000673.1:g.64527468del GRCh37
NC_000011.8:g.64284044del NCBI36
NG_013018.1:g.5723del

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.3:c.-95del ENSP00000164139.3:n.-95del
NM_001164716.1:c.-95del NP_001158188.1:n.-95del
NM_005609.2:c.-95del NP_005600.1:n.-95del
NM_005609.3:c.-95del NP_005600.1:n.-95del
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