Canonical Allele Identifier: CA381112904
Gene: PYGM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759804A>G , CM000673.2:g.64759804A>G GRCh38
NC_000011.9:g.64527276A>G , CM000673.1:g.64527276A>G GRCh37
NC_000011.8:g.64283852A>G NCBI36
NG_013018.1:g.5912T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.95T>C MANE Select ENSP00000164139.3:p.Phe32Ser
ENST00000164139.3:c.95T>C ENSP00000164139.3:p.Phe32Ser
ENST00000377432.7:c.95T>C ENSP00000366650.3:p.Phe32Ser
NM_001164716.1:c.95T>C NP_001158188.1:p.Phe32Ser
NM_005609.2:c.95T>C NP_005600.1:p.Phe32Ser
NM_005609.3:c.95T>C NP_005600.1:p.Phe32Ser
NM_005609.4:c.95T>C MANE Select NP_005600.1:p.Phe32Ser