Canonical Allele Identifier: CA9174491

Gene: OR7G3

Linked Data

• dbSNP Id: rs774392604
• ExAC: 19:9236959 G / T
• gnomAD v2: 19-9236959-G-T
• gnomAD v3: 19-9126283-G-T
• gnomAD v4: 19-9126283-G-T
• MyVariant Identifiers: chr19:g.9236959G>T (hg19) ; chr19:g.9126283G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126283G>T , CM000681.2:g.9126283G>T	GRCh38
NC_000019.9:g.9236959G>T , CM000681.1:g.9236959G>T	GRCh37
NC_000019.8:g.9097959G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.668C>A MANE Select	ENSP00000302867.2:p.Ser223Tyr
NM_001001958.1:c.668C>A MANE Select	NP_001001958.1:p.Ser223Tyr