Canonical Allele Identifier: CA419188165
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs1243640041
gnomAD v2: 1-101005545-G-A
gnomAD v3: 1-100539989-G-A
gnomAD v4: 1-100539989-G-A
MyVariant Identifiers: chr1:g.101005545G>A (hg19) chr1:g.100539989G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539989G>A , CM000663.2:g.100539989G>A GRCh38
NC_000001.10:g.101005545G>A , CM000663.1:g.101005545G>A GRCh37
NC_000001.9:g.100778133G>A NCBI36
NG_053134.1:g.6818G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1023G>A MANE Select ENSP00000314223.4:p.Glu341=
ENST00000315033.4:c.1023G>A ENSP00000314223.4:p.Glu341=
NM_022049.2:c.1023G>A NP_071332.2:p.Glu341=
NM_022049.3:c.1023G>A MANE Select NP_071332.2:p.Glu341=
Search 100 bp 5'
Search 100 bp 3'