Canonical Allele Identifier: CA2321774949
Gene: OR7G3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126300A= , CM000681.2:g.9126300A= GRCh38
NC_000019.9:g.9236976A= , CM000681.1:g.9236976A= GRCh37
NC_000019.8:g.9097976A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.651T= MANE Select ENSP00000302867.2:p.Ser217=
NM_001001958.1:c.651T= MANE Select NP_001001958.1:p.Ser217=
Search 100 bp 5'
Search 100 bp 3'