Canonical Allele Identifier: CA631707302
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs1350703143
gnomAD v2: 19-9237173-TAAC-T
gnomAD v4: 19-9126497-TAAC-T
MyVariant Identifiers: chr19:g.9237174_9237176del (hg19) chr19:g.9126498_9126500del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126498_9126500del , CM000681.2:g.9126498_9126500del GRCh38
NC_000019.9:g.9237174_9237176del , CM000681.1:g.9237174_9237176del GRCh37
NC_000019.8:g.9098174_9098176del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.451_453del MANE Select ENSP00000302867.2:p.Val151del
NM_001001958.1:c.451_453del MANE Select NP_001001958.1:p.Val151del
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