Canonical Allele Identifier: CA419317457
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs1651698668
MyVariant Identifiers: chr1:g.101005137A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539581A>C , CM000663.2:g.100539581A>C GRCh38
NC_000001.10:g.101005137A>C , CM000663.1:g.101005137A>C GRCh37
NC_000001.9:g.100777725A>C NCBI36
NG_053134.1:g.6410A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.615A>C MANE Select ENSP00000314223.4:p.Thr205=
ENST00000315033.4:c.615A>C ENSP00000314223.4:p.Thr205=
NM_022049.2:c.615A>C NP_071332.2:p.Thr205=
NM_022049.3:c.615A>C MANE Select NP_071332.2:p.Thr205=
Search 100 bp 5'
Search 100 bp 3'