Canonical Allele Identifier: CA403805391
Gene: OR7D4 HGNC NCBI

Linked Data

dbSNP Id: rs1599222326
MyVariant Identifiers: chr19:g.9325131T>G (hg19) chr19:g.9214455T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9214455T>G , CM000681.2:g.9214455T>G GRCh38
NC_000019.9:g.9325131T>G , CM000681.1:g.9325131T>G GRCh37
NC_000019.8:g.9186131T>G NCBI36
NG_027953.1:g.5417A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000641244.1:c.383A>C ENSP00000493404.1:p.His128Pro
ENST00000641669.1:c.383A>C MANE Select ENSP00000493383.1:p.His128Pro
ENST00000308682.3:c.383A>C ENSP00000310488.2:p.His128Pro
NM_001005191.2:c.383A>C NP_001005191.1:p.His128Pro
NM_001005191.3:c.383A>C MANE Select NP_001005191.1:p.His128Pro
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