Canonical Allele Identifier: CA403791832
Gene: OR7G3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.9237608A>T (hg19) chr19:g.9126932A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126932A>T , CM000681.2:g.9126932A>T GRCh38
NC_000019.9:g.9237608A>T , CM000681.1:g.9237608A>T GRCh37
NC_000019.8:g.9098608A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.19T>A MANE Select ENSP00000302867.2:p.Ser7Thr
NM_001001958.1:c.19T>A MANE Select NP_001001958.1:p.Ser7Thr
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