Canonical Allele Identifier: CA403786089
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs1390472697
gnomAD v3: 19-9126272-T-G
gnomAD v4: 19-9126272-T-G
MyVariant Identifiers: chr19:g.9236948T>G (hg19) chr19:g.9126272T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126272T>G , CM000681.2:g.9126272T>G GRCh38
NC_000019.9:g.9236948T>G , CM000681.1:g.9236948T>G GRCh37
NC_000019.8:g.9097948T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.679A>C MANE Select ENSP00000302867.2:p.Lys227Gln
NM_001001958.1:c.679A>C MANE Select NP_001001958.1:p.Lys227Gln
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Search 100 bp 3'