Canonical Allele Identifier: CA505454784
Gene: OR7D4 HGNC NCBI

Linked Data

dbSNP Id: rs1218305215
gnomAD v2: 19-9325031-T-A
gnomAD v4: 19-9214355-T-A
MyVariant Identifiers: chr19:g.9325031T>A (hg19) chr19:g.9214355T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9214355T>A , CM000681.2:g.9214355T>A GRCh38
NC_000019.9:g.9325031T>A , CM000681.1:g.9325031T>A GRCh37
NC_000019.8:g.9186031T>A NCBI36
NG_027953.1:g.5517A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000641244.1:c.483A>T ENSP00000493404.1:p.Leu161=
ENST00000641669.1:c.483A>T MANE Select ENSP00000493383.1:p.Leu161=
ENST00000308682.3:c.483A>T ENSP00000310488.2:p.Leu161=
NM_001005191.2:c.483A>T NP_001005191.1:p.Leu161=
NM_001005191.3:c.483A>T MANE Select NP_001005191.1:p.Leu161=
Search 100 bp 5'
Search 100 bp 3'