Canonical Allele Identifier: CA9175374
Gene: OR7D4 HGNC NCBI

Linked Data

dbSNP Id: rs775966397
ExAC: 19:9324932 G / C
gnomAD v2: 19-9324932-G-C
gnomAD v3: 19-9214256-G-C
gnomAD v4: 19-9214256-G-C
MyVariant Identifiers: chr19:g.9324932G>C (hg19) chr19:g.9214256G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9214256G>C , CM000681.2:g.9214256G>C GRCh38
NC_000019.9:g.9324932G>C , CM000681.1:g.9324932G>C GRCh37
NC_000019.8:g.9185932G>C NCBI36
NG_027953.1:g.5616C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000641244.1:c.582C>G ENSP00000493404.1:p.Leu194=
ENST00000641669.1:c.582C>G MANE Select ENSP00000493383.1:p.Leu194=
ENST00000308682.3:c.582C>G ENSP00000310488.2:p.Leu194=
NM_001005191.2:c.582C>G NP_001005191.1:p.Leu194=
NM_001005191.3:c.582C>G MANE Select NP_001005191.1:p.Leu194=
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