Canonical Allele Identifier: CA9174606

Gene: OR7G3

Linked Data

• dbSNP Id: rs762770060
• ExAC: 19:9237537 C / T
• gnomAD v2: 19-9237537-C-T
• gnomAD v4: 19-9126861-C-T
• MyVariant Identifiers: chr19:g.9237537C>T (hg19) ; chr19:g.9126861C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126861C>T , CM000681.2:g.9126861C>T	GRCh38
NC_000019.9:g.9237537C>T , CM000681.1:g.9237537C>T	GRCh37
NC_000019.8:g.9098537C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.90G>A MANE Select	ENSP00000302867.2:p.Leu30=
NM_001001958.1:c.90G>A MANE Select	NP_001001958.1:p.Leu30=