Canonical Allele Identifier: CA341392979
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs1651721768
gnomAD v4: 1-100539993-T-C
MyVariant Identifiers: chr1:g.101005549T>C (hg19) chr1:g.100539993T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539993T>C , CM000663.2:g.100539993T>C GRCh38
NC_000001.10:g.101005549T>C , CM000663.1:g.101005549T>C GRCh37
NC_000001.9:g.100778137T>C NCBI36
NG_053134.1:g.6822T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1027T>C MANE Select ENSP00000314223.4:p.Phe343Leu
ENST00000315033.4:c.1027T>C ENSP00000314223.4:p.Phe343Leu
NM_022049.2:c.1027T>C NP_071332.2:p.Phe343Leu
NM_022049.3:c.1027T>C MANE Select NP_071332.2:p.Phe343Leu
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