Canonical Allele Identifier: CA341392510
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs1221791377
gnomAD v3: 1-100539765-C-G
gnomAD v4: 1-100539765-C-G
MyVariant Identifiers: chr1:g.101005321C>G (hg19) chr1:g.100539765C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539765C>G , CM000663.2:g.100539765C>G GRCh38
NC_000001.10:g.101005321C>G , CM000663.1:g.101005321C>G GRCh37
NC_000001.9:g.100777909C>G NCBI36
NG_053134.1:g.6594C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.799C>G MANE Select ENSP00000314223.4:p.Pro267Ala
ENST00000315033.4:c.799C>G ENSP00000314223.4:p.Pro267Ala
NM_022049.2:c.799C>G NP_071332.2:p.Pro267Ala
NM_022049.3:c.799C>G MANE Select NP_071332.2:p.Pro267Ala
Search 100 bp 5'
Search 100 bp 3'