Canonical Allele Identifier: CA631707320
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs1568305319
gnomAD v2: 19-9237024-C-CAAATACACCAGGATGTAAAAGGCGAAAGATTTATTCGATCTGAAGAGAAACCAGTGTAATA
gnomAD v3: 19-9126348-C-CAAATACACCAGGATGTAAAAGGCGAAAGATTTATTCGATCTGAAGAGAAACCAGTGTAATA
gnomAD v4: 19-9126348-C-CAAATACACCAGGATGTAAAAGGCGAAAGATTTATTCGATCTGAAGAGAAACCAGTGTAATA
MyVariant Identifiers: chr19:g.9237024_9237025insAAATACACCAGGATGTAAAAGGCGAAAGATTTATTCGATCTGAAGAGAAACCAGTGTAATA (hg19) chr19:g.9126348_9126349insAAATACACCAGGATGTAAAAGGCGAAAGATTTATTCGATCTGAAGAGAAACCAGTGTAATA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126364_9126365insAAAAGGCGAAAGATTTATTCGATCTGAAGAGAAACCAGTGTAATAAAATACACCAGGATGT , CM000681.2:g.9126364_9126365insAAAAGGCGAAAGATTTATTCGATCTGAAGAGAAACCAGTGTAATAAAATACACCAGGATGT GRCh38
NC_000019.9:g.9237040_9237041insAAAAGGCGAAAGATTTATTCGATCTGAAGAGAAACCAGTGTAATAAAATACACCAGGATGT , CM000681.1:g.9237040_9237041insAAAAGGCGAAAGATTTATTCGATCTGAAGAGAAACCAGTGTAATAAAATACACCAGGATGT GRCh37
NC_000019.8:g.9098040_9098041insAAAAGGCGAAAGATTTATTCGATCTGAAGAGAAACCAGTGTAATAAAATACACCAGGATGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.602_603insTATTACACTGGTTTCTCTTCAGATCGAATAAATCTTTCGCCTTTTACATCCTGGTGTATTT MANE Select ENSP00000302867.2:p.Leu201PhefsTer11
NM_001001958.1:c.602_603insTATTACACTGGTTTCTCTTCAGATCGAATAAATCTTTCGCCTTTTACATCCTGGTGTATTT MANE Select NP_001001958.1:p.Leu201PhefsTer11
Search 100 bp 5'
Search 100 bp 3'