Canonical Allele Identifier: CA305051122
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs1011096245
COSMIC: COSM3363107
MyVariant Identifiers: chr19:g.9237030C>A (hg19) chr19:g.9126354C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126354C>A , CM000681.2:g.9126354C>A GRCh38
NC_000019.9:g.9237030C>A , CM000681.1:g.9237030C>A GRCh37
NC_000019.8:g.9098030C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.597G>T MANE Select ENSP00000302867.2:p.Val199=
NM_001001958.1:c.597G>T MANE Select NP_001001958.1:p.Val199=
Search 100 bp 5'
Search 100 bp 3'