Canonical Allele Identifier: CA341392298

Gene: GPR88

Linked Data

• gnomAD v4: 1-100539663-C-G
• MyVariant Identifiers: chr1:g.101005219C>G (hg19) ; chr1:g.100539663C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100539663C>G , CM000663.2:g.100539663C>G	GRCh38
NC_000001.10:g.101005219C>G , CM000663.1:g.101005219C>G	GRCh37
NC_000001.9:g.100777807C>G	NCBI36
NG_053134.1:g.6492C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315033.5:c.697C>G MANE Select	ENSP00000314223.4:p.Leu233Val
ENST00000315033.4:c.697C>G	ENSP00000314223.4:p.Leu233Val
NM_022049.2:c.697C>G	NP_071332.2:p.Leu233Val
NM_022049.3:c.697C>G MANE Select	NP_071332.2:p.Leu233Val