Canonical Allele Identifier: CA341392751
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs1402406870
gnomAD v2: 1-101005442-G-C
MyVariant Identifiers: chr1:g.101005442G>C (hg19) chr1:g.100539886G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539886G>C , CM000663.2:g.100539886G>C GRCh38
NC_000001.10:g.101005442G>C , CM000663.1:g.101005442G>C GRCh37
NC_000001.9:g.100778030G>C NCBI36
NG_053134.1:g.6715G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.920G>C MANE Select ENSP00000314223.4:p.Ser307Thr
ENST00000315033.4:c.920G>C ENSP00000314223.4:p.Ser307Thr
NM_022049.2:c.920G>C NP_071332.2:p.Ser307Thr
NM_022049.3:c.920G>C MANE Select NP_071332.2:p.Ser307Thr
Search 100 bp 5'
Search 100 bp 3'