Canonical Allele Identifier: CA403804718
Gene: OR7D4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.9325029A>T (hg19) chr19:g.9214353A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9214353A>T , CM000681.2:g.9214353A>T GRCh38
NC_000019.9:g.9325029A>T , CM000681.1:g.9325029A>T GRCh37
NC_000019.8:g.9186029A>T NCBI36
NG_027953.1:g.5519T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000641244.1:c.485T>A ENSP00000493404.1:p.Leu162Gln
ENST00000641669.1:c.485T>A MANE Select ENSP00000493383.1:p.Leu162Gln
ENST00000308682.3:c.485T>A ENSP00000310488.2:p.Leu162Gln
NM_001005191.2:c.485T>A NP_001005191.1:p.Leu162Gln
NM_001005191.3:c.485T>A MANE Select NP_001005191.1:p.Leu162Gln
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