Canonical Allele Identifier: CA505453139
Gene: OR7G3 HGNC NCBI

Linked Data

gnomAD v4: 19-9126642-A-G
MyVariant Identifiers: chr19:g.9237318A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126642A>G , CM000681.2:g.9126642A>G GRCh38
NC_000019.9:g.9237318A>G , CM000681.1:g.9237318A>G GRCh37
NC_000019.8:g.9098318A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.309T>C MANE Select ENSP00000302867.2:p.Phe103=
NM_001001958.1:c.309T>C MANE Select NP_001001958.1:p.Phe103=