Canonical Allele Identifier: CA505453302
Gene: OR7G3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.9237606T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126930T>G , CM000681.2:g.9126930T>G GRCh38
NC_000019.9:g.9237606T>G , CM000681.1:g.9237606T>G GRCh37
NC_000019.8:g.9098606T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.21A>C MANE Select ENSP00000302867.2:p.Ser7=
NM_001001958.1:c.21A>C MANE Select NP_001001958.1:p.Ser7=
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