Canonical Allele Identifier: CA341392732
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539877-G-T
MyVariant Identifiers: chr1:g.101005433G>T (hg19) chr1:g.100539877G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539877G>T , CM000663.2:g.100539877G>T GRCh38
NC_000001.10:g.101005433G>T , CM000663.1:g.101005433G>T GRCh37
NC_000001.9:g.100778021G>T NCBI36
NG_053134.1:g.6706G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.911G>T MANE Select ENSP00000314223.4:p.Ser304Ile
ENST00000315033.4:c.911G>T ENSP00000314223.4:p.Ser304Ile
NM_022049.2:c.911G>T NP_071332.2:p.Ser304Ile
NM_022049.3:c.911G>T MANE Select NP_071332.2:p.Ser304Ile
Search 100 bp 5'
Search 100 bp 3'