Canonical Allele Identifier: CA341392151
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539595-A-C
MyVariant Identifiers: chr1:g.101005151A>C (hg19) chr1:g.100539595A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539595A>C , CM000663.2:g.100539595A>C GRCh38
NC_000001.10:g.101005151A>C , CM000663.1:g.101005151A>C GRCh37
NC_000001.9:g.100777739A>C NCBI36
NG_053134.1:g.6424A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.629A>C MANE Select ENSP00000314223.4:p.His210Pro
ENST00000315033.4:c.629A>C ENSP00000314223.4:p.His210Pro
NM_022049.2:c.629A>C NP_071332.2:p.His210Pro
NM_022049.3:c.629A>C MANE Select NP_071332.2:p.His210Pro
Search 100 bp 5'
Search 100 bp 3'