Canonical Allele Identifier: CA341393006
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs1440728591
gnomAD v2: 1-101005562-T-C
gnomAD v3: 1-100540006-T-C
gnomAD v4: 1-100540006-T-C
MyVariant Identifiers: chr1:g.101005562T>C (hg19) chr1:g.100540006T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100540006T>C , CM000663.2:g.100540006T>C GRCh38
NC_000001.10:g.101005562T>C , CM000663.1:g.101005562T>C GRCh37
NC_000001.9:g.100778150T>C NCBI36
NG_053134.1:g.6835T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1040T>C MANE Select ENSP00000314223.4:p.Val347Ala
ENST00000315033.4:c.1040T>C ENSP00000314223.4:p.Val347Ala
NM_022049.2:c.1040T>C NP_071332.2:p.Val347Ala
NM_022049.3:c.1040T>C MANE Select NP_071332.2:p.Val347Ala
Search 100 bp 5'
Search 100 bp 3'