Canonical Allele Identifier: CA6080232
Gene: PYGM HGNC NCBI

Linked Data

ClinVar Variation Id: 2850187
ClinVar RCV Id: RCV003604893
dbSNP Id: rs771328699

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64758252G>A , CM000673.2:g.64758252G>A GRCh38
NC_000011.9:g.64525724G>A , CM000673.1:g.64525724G>A GRCh37
NC_000011.8:g.64282300G>A NCBI36
NG_013018.1:g.7464C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.522C>T MANE Select ENSP00000164139.3:p.Gly174=
ENST00000164139.3:c.522C>T ENSP00000164139.3:p.Gly174=
ENST00000377432.7:c.258C>T ENSP00000366650.3:p.Gly86=
NM_001164716.1:c.258C>T NP_001158188.1:p.Gly86=
NM_005609.2:c.522C>T NP_005600.1:p.Gly174=
NM_005609.3:c.522C>T NP_005600.1:p.Gly174=
NM_005609.4:c.522C>T MANE Select NP_005600.1:p.Gly174=