Canonical Allele Identifier: CA920054961
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs1568305321
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126355dup , CM000681.2:g.9126355dup GRCh38
NC_000019.9:g.9237031dup , CM000681.1:g.9237031dup GRCh37
NC_000019.8:g.9098031dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.596dup MANE Select ENSP00000302867.2:p.Tyr200ValfsTer?
NM_001001958.1:c.596dup MANE Select NP_001001958.1:p.Tyr200ValfsTer?
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Search 100 bp 3'