Canonical Allele Identifier: CA938864577
Gene: PYGM HGNC NCBI

Linked Data

dbSNP Id: rs2058349731

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64750607A>C , CM000673.2:g.64750607A>C GRCh38
NC_000011.9:g.64518079A>C , CM000673.1:g.64518079A>C GRCh37
NC_000011.8:g.64274655A>C NCBI36
NG_013018.1:g.15109T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000164139.4:c.1970-24T>G MANE Select ENSP00000164139.3:n.1970-24T>G
ENST00000164139.3:c.1970-24T>G ENSP00000164139.3:n.1970-24T>G
ENST00000377432.7:c.1706-24T>G ENSP00000366650.3:n.1706-24T>G
NM_001164716.1:c.1706-24T>G NP_001158188.1:n.1706-24T>G
NM_005609.2:c.1970-24T>G NP_005600.1:n.1970-24T>G
NM_005609.3:c.1970-24T>G NP_005600.1:n.1970-24T>G
NM_005609.4:c.1970-24T>G MANE Select NP_005600.1:n.1970-24T>G