Canonical Allele Identifier: CA2321774948
Gene: OR7G3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126299A= , CM000681.2:g.9126299A= GRCh38
NC_000019.9:g.9236975A= , CM000681.1:g.9236975A= GRCh37
NC_000019.8:g.9097975A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.652T= MANE Select ENSP00000302867.2:p.Tyr218=
NM_001001958.1:c.652T= MANE Select NP_001001958.1:p.Tyr218=
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