Canonical Allele Identifier: CA1978930199
Gene: PYGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759992A= , CM000673.2:g.64759992A= GRCh38
NC_000011.9:g.64527464A= , CM000673.1:g.64527464A= GRCh37
NC_000011.8:g.64284040A= NCBI36
NG_013018.1:g.5724T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.3:c.-94T= ENSP00000164139.3:n.-94T=
NM_001164716.1:c.-94T= NP_001158188.1:n.-94T=
NM_005609.2:c.-94T= NP_005600.1:n.-94T=
NM_005609.3:c.-94T= NP_005600.1:n.-94T=