Canonical Allele Identifier: CA9174495

Gene: OR7G3

Linked Data

• dbSNP Id: rs758178089
• ExAC: 19:9236966 T / C
• gnomAD v2: 19-9236966-T-C
• gnomAD v3: 19-9126290-T-C
• gnomAD v4: 19-9126290-T-C
• MyVariant Identifiers: chr19:g.9236966T>C (hg19) ; chr19:g.9126290T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126290T>C , CM000681.2:g.9126290T>C	GRCh38
NC_000019.9:g.9236966T>C , CM000681.1:g.9236966T>C	GRCh37
NC_000019.8:g.9097966T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.661A>G MANE Select	ENSP00000302867.2:p.Ile221Val
NM_001001958.1:c.661A>G MANE Select	NP_001001958.1:p.Ile221Val