Canonical Allele Identifier: CA403791766
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs1197384227
gnomAD v3: 19-9126925-G-C
gnomAD v4: 19-9126925-G-C
MyVariant Identifiers: chr19:g.9237601G>C (hg19) chr19:g.9126925G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126925G>C , CM000681.2:g.9126925G>C GRCh38
NC_000019.9:g.9237601G>C , CM000681.1:g.9237601G>C GRCh37
NC_000019.8:g.9098601G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.26C>G MANE Select ENSP00000302867.2:p.Thr9Ser
NM_001001958.1:c.26C>G MANE Select NP_001001958.1:p.Thr9Ser
Search 100 bp 5'
Search 100 bp 3'