Canonical Allele Identifier: CA9174533
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs759580069
ExAC: 19:9237137 G / GC
gnomAD v2: 19-9237137-G-GC
gnomAD v4: 19-9126461-G-GC
MyVariant Identifiers: chr19:g.9237137_9237138insC (hg19) chr19:g.9126461_9126462insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126462dup , CM000681.2:g.9126462dup GRCh38
NC_000019.9:g.9237138dup , CM000681.1:g.9237138dup GRCh37
NC_000019.8:g.9098138dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.489dup MANE Select ENSP00000302867.2:p.Leu164AlafsTer17
NM_001001958.1:c.489dup MANE Select NP_001001958.1:p.Leu164AlafsTer17
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