Canonical Allele Identifier: CA971147
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs762781426

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539971C>G , CM000663.2:g.100539971C>G GRCh38
NC_000001.10:g.101005527C>G , CM000663.1:g.101005527C>G GRCh37
NC_000001.9:g.100778115C>G NCBI36
NG_053134.1:g.6800C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1005C>G MANE Select ENSP00000314223.4:p.Leu335=
ENST00000315033.4:c.1005C>G ENSP00000314223.4:p.Leu335=
NM_022049.2:c.1005C>G NP_071332.2:p.Leu335=
NM_022049.3:c.1005C>G MANE Select NP_071332.2:p.Leu335=