Canonical Allele Identifier: CA419188142
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs1471938009
gnomAD v2: 1-101005506-G-T
gnomAD v4: 1-100539950-G-T
MyVariant Identifiers: chr1:g.101005506G>T (hg19) chr1:g.100539950G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539950G>T , CM000663.2:g.100539950G>T GRCh38
NC_000001.10:g.101005506G>T , CM000663.1:g.101005506G>T GRCh37
NC_000001.9:g.100778094G>T NCBI36
NG_053134.1:g.6779G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.984G>T MANE Select ENSP00000314223.4:p.Leu328=
ENST00000315033.4:c.984G>T ENSP00000314223.4:p.Leu328=
NM_022049.2:c.984G>T NP_071332.2:p.Leu328=
NM_022049.3:c.984G>T MANE Select NP_071332.2:p.Leu328=
Search 100 bp 5'
Search 100 bp 3'