Canonical Allele Identifier: CA9174547
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs763840296
gnomAD v2: 19-9237216-G-T
gnomAD v4: 19-9126540-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126540G>T , CM000681.2:g.9126540G>T GRCh38
NC_000019.9:g.9237216G>T , CM000681.1:g.9237216G>T GRCh37
NC_000019.8:g.9098216G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.411C>A MANE Select ENSP00000302867.2:p.Asn137Lys
NM_001001958.1:c.411C>A MANE Select NP_001001958.1:p.Asn137Lys