Canonical Allele Identifier: CA403788187
Gene: OR7G3 HGNC NCBI

Linked Data

gnomAD v4: 19-9126553-T-C
MyVariant Identifiers: chr19:g.9237229T>C (hg19) chr19:g.9126553T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126553T>C , CM000681.2:g.9126553T>C GRCh38
NC_000019.9:g.9237229T>C , CM000681.1:g.9237229T>C GRCh37
NC_000019.8:g.9098229T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.398A>G MANE Select ENSP00000302867.2:p.Asn133Ser
NM_001001958.1:c.398A>G MANE Select NP_001001958.1:p.Asn133Ser
Search 100 bp 5'
Search 100 bp 3'