Canonical Allele Identifier: CA341392192
Gene: GPR88 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539613T>C , CM000663.2:g.100539613T>C GRCh38
NC_000001.10:g.101005169T>C , CM000663.1:g.101005169T>C GRCh37
NC_000001.9:g.100777757T>C NCBI36
NG_053134.1:g.6442T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.647T>C MANE Select ENSP00000314223.4:p.Val216Ala
ENST00000315033.4:c.647T>C ENSP00000314223.4:p.Val216Ala
NM_022049.2:c.647T>C NP_071332.2:p.Val216Ala
NM_022049.3:c.647T>C MANE Select NP_071332.2:p.Val216Ala