Canonical Allele Identifier: CA2614192154
Gene: PYGM HGNC NCBI

Linked Data

gnomAD v4: 11-64759990-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759990C>G , CM000673.2:g.64759990C>G GRCh38
NC_000011.9:g.64527462C>G , CM000673.1:g.64527462C>G GRCh37
NC_000011.8:g.64284038C>G NCBI36
NG_013018.1:g.5726G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.3:c.-92G>C ENSP00000164139.3:n.-92G>C
NM_001164716.1:c.-92G>C NP_001158188.1:n.-92G>C
NM_005609.2:c.-92G>C NP_005600.1:n.-92G>C
NM_005609.3:c.-92G>C NP_005600.1:n.-92G>C
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