Canonical Allele Identifier: CA341392132
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs1450370459
gnomAD v2: 1-101005139-C-G
MyVariant Identifiers: chr1:g.101005139C>G (hg19) chr1:g.100539583C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539583C>G , CM000663.2:g.100539583C>G GRCh38
NC_000001.10:g.101005139C>G , CM000663.1:g.101005139C>G GRCh37
NC_000001.9:g.100777727C>G NCBI36
NG_053134.1:g.6412C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.617C>G MANE Select ENSP00000314223.4:p.Ala206Gly
ENST00000315033.4:c.617C>G ENSP00000314223.4:p.Ala206Gly
NM_022049.2:c.617C>G NP_071332.2:p.Ala206Gly
NM_022049.3:c.617C>G MANE Select NP_071332.2:p.Ala206Gly
Search 100 bp 5'
Search 100 bp 3'