Canonical Allele Identifier: CA403805297
Gene: OR7D4 HGNC NCBI

Linked Data

dbSNP Id: rs1337655451
gnomAD v2: 19-9325120-A-G
gnomAD v4: 19-9214444-A-G
MyVariant Identifiers: chr19:g.9325120A>G (hg19) chr19:g.9214444A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9214444A>G , CM000681.2:g.9214444A>G GRCh38
NC_000019.9:g.9325120A>G , CM000681.1:g.9325120A>G GRCh37
NC_000019.8:g.9186120A>G NCBI36
NG_027953.1:g.5428T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000641244.1:c.394T>C ENSP00000493404.1:p.Tyr132His
ENST00000641669.1:c.394T>C MANE Select ENSP00000493383.1:p.Tyr132His
ENST00000308682.3:c.394T>C ENSP00000310488.2:p.Tyr132His
NM_001005191.2:c.394T>C NP_001005191.1:p.Tyr132His
NM_001005191.3:c.394T>C MANE Select NP_001005191.1:p.Tyr132His
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