Canonical Allele Identifier: CA341392349

Gene: GPR88

Linked Data

• gnomAD v4: 1-100539687-G-C
• MyVariant Identifiers: chr1:g.101005243G>C (hg19) ; chr1:g.100539687G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100539687G>C , CM000663.2:g.100539687G>C	GRCh38
NC_000001.10:g.101005243G>C , CM000663.1:g.101005243G>C	GRCh37
NC_000001.9:g.100777831G>C	NCBI36
NG_053134.1:g.6516G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315033.5:c.721G>C MANE Select	ENSP00000314223.4:p.Ala241Pro
ENST00000315033.4:c.721G>C	ENSP00000314223.4:p.Ala241Pro
NM_022049.2:c.721G>C	NP_071332.2:p.Ala241Pro
NM_022049.3:c.721G>C MANE Select	NP_071332.2:p.Ala241Pro