Canonical Allele Identifier: CA341392094
Gene: GPR88 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.101005120G>C (hg19) chr1:g.100539564G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539564G>C , CM000663.2:g.100539564G>C GRCh38
NC_000001.10:g.101005120G>C , CM000663.1:g.101005120G>C GRCh37
NC_000001.9:g.100777708G>C NCBI36
NG_053134.1:g.6393G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.598G>C MANE Select ENSP00000314223.4:p.Ala200Pro
ENST00000315033.4:c.598G>C ENSP00000314223.4:p.Ala200Pro
NM_022049.2:c.598G>C NP_071332.2:p.Ala200Pro
NM_022049.3:c.598G>C MANE Select NP_071332.2:p.Ala200Pro
Search 100 bp 5'
Search 100 bp 3'