Canonical Allele Identifier: CA1978930213
Gene: PYGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64760017C= , CM000673.2:g.64760017C= GRCh38
NC_000011.9:g.64527489C= , CM000673.1:g.64527489C= GRCh37
NC_000011.8:g.64284065C= NCBI36
NG_013018.1:g.5699G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.3:c.-119G= ENSP00000164139.3:n.-119G=
NM_001164716.1:c.-119G= NP_001158188.1:n.-119G=
NM_005609.2:c.-119G= NP_005600.1:n.-119G=
NM_005609.3:c.-119G= NP_005600.1:n.-119G=