Canonical Allele Identifier: CA381167646
Gene: PYGM HGNC NCBI

Linked Data

dbSNP Id: rs1285381507

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64750433T>C , CM000673.2:g.64750433T>C GRCh38
NC_000011.9:g.64517905T>C , CM000673.1:g.64517905T>C GRCh37
NC_000011.8:g.64274481T>C NCBI36
NG_007574.1:g.24A>G , LRG_100:g.24A>G
NG_013018.1:g.15283A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.2120A>G MANE Select ENSP00000164139.3:p.Glu707Gly
ENST00000164139.3:c.2120A>G ENSP00000164139.3:p.Glu707Gly
ENST00000377432.7:c.1856A>G ENSP00000366650.3:p.Glu619Gly
NM_001164716.1:c.1856A>G NP_001158188.1:p.Glu619Gly
NM_005609.2:c.2120A>G NP_005600.1:p.Glu707Gly
NM_005609.3:c.2120A>G NP_005600.1:p.Glu707Gly
NM_005609.4:c.2120A>G MANE Select NP_005600.1:p.Glu707Gly