Canonical Allele Identifier: CA341392158
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs1311673019
gnomAD v2: 1-101005154-G-C
gnomAD v4: 1-100539598-G-C
MyVariant Identifiers: chr1:g.101005154G>C (hg19) chr1:g.100539598G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539598G>C , CM000663.2:g.100539598G>C GRCh38
NC_000001.10:g.101005154G>C , CM000663.1:g.101005154G>C GRCh37
NC_000001.9:g.100777742G>C NCBI36
NG_053134.1:g.6427G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.632G>C MANE Select ENSP00000314223.4:p.Cys211Ser
ENST00000315033.4:c.632G>C ENSP00000314223.4:p.Cys211Ser
NM_022049.2:c.632G>C NP_071332.2:p.Cys211Ser
NM_022049.3:c.632G>C MANE Select NP_071332.2:p.Cys211Ser
Search 100 bp 5'
Search 100 bp 3'