Canonical Allele Identifier: CA341392175
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539604-T-A
MyVariant Identifiers: chr1:g.101005160T>A (hg19) chr1:g.100539604T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539604T>A , CM000663.2:g.100539604T>A GRCh38
NC_000001.10:g.101005160T>A , CM000663.1:g.101005160T>A GRCh37
NC_000001.9:g.100777748T>A NCBI36
NG_053134.1:g.6433T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.638T>A MANE Select ENSP00000314223.4:p.Leu213Gln
ENST00000315033.4:c.638T>A ENSP00000314223.4:p.Leu213Gln
NM_022049.2:c.638T>A NP_071332.2:p.Leu213Gln
NM_022049.3:c.638T>A MANE Select NP_071332.2:p.Leu213Gln
Search 100 bp 5'
Search 100 bp 3'