Canonical Allele Identifier: CA403805686
Gene: OR7D4 HGNC NCBI

Linked Data

dbSNP Id: rs751657242
MyVariant Identifiers: chr19:g.9325168C>G (hg19) chr19:g.9214492C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9214492C>G , CM000681.2:g.9214492C>G GRCh38
NC_000019.9:g.9325168C>G , CM000681.1:g.9325168C>G GRCh37
NC_000019.8:g.9186168C>G NCBI36
NG_027953.1:g.5380G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000641244.1:c.346G>C ENSP00000493404.1:p.Ala116Pro
ENST00000641669.1:c.346G>C MANE Select ENSP00000493383.1:p.Ala116Pro
ENST00000308682.3:c.346G>C ENSP00000310488.2:p.Ala116Pro
NM_001005191.2:c.346G>C NP_001005191.1:p.Ala116Pro
NM_001005191.3:c.346G>C MANE Select NP_001005191.1:p.Ala116Pro
Search 100 bp 5'
Search 100 bp 3'