Canonical Allele Identifier: CA403804697
Gene: OR7D4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.9325024T>G (hg19) chr19:g.9214348T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9214348T>G , CM000681.2:g.9214348T>G GRCh38
NC_000019.9:g.9325024T>G , CM000681.1:g.9325024T>G GRCh37
NC_000019.8:g.9186024T>G NCBI36
NG_027953.1:g.5524A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000641244.1:c.490A>C ENSP00000493404.1:p.Lys164Gln
ENST00000641669.1:c.490A>C MANE Select ENSP00000493383.1:p.Lys164Gln
ENST00000308682.3:c.490A>C ENSP00000310488.2:p.Lys164Gln
NM_001005191.2:c.490A>C NP_001005191.1:p.Lys164Gln
NM_001005191.3:c.490A>C MANE Select NP_001005191.1:p.Lys164Gln
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