Canonical Allele Identifier: CA341392812

Gene: GPR88

Linked Data

• gnomAD v4: 1-100539916-T-C
• MyVariant Identifiers: chr1:g.101005472T>C (hg19) ; chr1:g.100539916T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100539916T>C , CM000663.2:g.100539916T>C	GRCh38
NC_000001.10:g.101005472T>C , CM000663.1:g.101005472T>C	GRCh37
NC_000001.9:g.100778060T>C	NCBI36
NG_053134.1:g.6745T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315033.5:c.950T>C MANE Select	ENSP00000314223.4:p.Val317Ala
ENST00000315033.4:c.950T>C	ENSP00000314223.4:p.Val317Ala
NM_022049.2:c.950T>C	NP_071332.2:p.Val317Ala
NM_022049.3:c.950T>C MANE Select	NP_071332.2:p.Val317Ala