Canonical Allele Identifier: CA341392190
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539612-G-C
MyVariant Identifiers: chr1:g.101005168G>C (hg19) chr1:g.100539612G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539612G>C , CM000663.2:g.100539612G>C GRCh38
NC_000001.10:g.101005168G>C , CM000663.1:g.101005168G>C GRCh37
NC_000001.9:g.100777756G>C NCBI36
NG_053134.1:g.6441G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.646G>C MANE Select ENSP00000314223.4:p.Val216Leu
ENST00000315033.4:c.646G>C ENSP00000314223.4:p.Val216Leu
NM_022049.2:c.646G>C NP_071332.2:p.Val216Leu
NM_022049.3:c.646G>C MANE Select NP_071332.2:p.Val216Leu
Search 100 bp 5'
Search 100 bp 3'