Canonical Allele Identifier: CA2614192162
Gene: PYGM HGNC NCBI

Linked Data

gnomAD v4: 11-64759996-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759996G>A , CM000673.2:g.64759996G>A GRCh38
NC_000011.9:g.64527468G>A , CM000673.1:g.64527468G>A GRCh37
NC_000011.8:g.64284044G>A NCBI36
NG_013018.1:g.5720C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.3:c.-98C>T ENSP00000164139.3:n.-98C>T
NM_001164716.1:c.-98C>T NP_001158188.1:n.-98C>T
NM_005609.2:c.-98C>T NP_005600.1:n.-98C>T
NM_005609.3:c.-98C>T NP_005600.1:n.-98C>T
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