Canonical Allele Identifier: CA2574865138
Gene: PYGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759977A>G , CM000673.2:g.64759977A>G GRCh38
NC_000011.9:g.64527449A>G , CM000673.1:g.64527449A>G GRCh37
NC_000011.8:g.64284025A>G NCBI36
NG_013018.1:g.5739T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.3:c.-79T>C ENSP00000164139.3:n.-79T>C
NM_001164716.1:c.-79T>C NP_001158188.1:n.-79T>C
NM_005609.2:c.-79T>C NP_005600.1:n.-79T>C
NM_005609.3:c.-79T>C NP_005600.1:n.-79T>C