Canonical Allele Identifier: CA1978929887
Gene: PYGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759751G= , CM000673.2:g.64759751G= GRCh38
NC_000011.9:g.64527223G= , CM000673.1:g.64527223G= GRCh37
NC_000011.8:g.64283799G= NCBI36
NG_013018.1:g.5965C=

Transcript Alleles

HGVS Amino-acid change
ENST00000164139.4:c.148C= MANE Select ENSP00000164139.3:p.Arg50=
ENST00000164139.3:c.148C= ENSP00000164139.3:p.Arg50=
ENST00000377432.7:c.148C= ENSP00000366650.3:p.Arg50=
NM_001164716.1:c.148C= NP_001158188.1:p.Arg50=
NM_005609.2:c.148C= NP_005600.1:p.Arg50=
NM_005609.3:c.148C= NP_005600.1:p.Arg50=
NM_005609.4:c.148C= MANE Select NP_005600.1:p.Arg50=