Canonical Allele Identifier: CA2614192155
Gene: PYGM HGNC NCBI

Linked Data

gnomAD v4: 11-64759991-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759991A>G , CM000673.2:g.64759991A>G GRCh38
NC_000011.9:g.64527463A>G , CM000673.1:g.64527463A>G GRCh37
NC_000011.8:g.64284039A>G NCBI36
NG_013018.1:g.5725T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.3:c.-93T>C ENSP00000164139.3:n.-93T>C
NM_001164716.1:c.-93T>C NP_001158188.1:n.-93T>C
NM_005609.2:c.-93T>C NP_005600.1:n.-93T>C
NM_005609.3:c.-93T>C NP_005600.1:n.-93T>C
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