Canonical Allele Identifier: CA2321816029
Gene: OR7D4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9214358A= , CM000681.2:g.9214358A= GRCh38
NC_000019.9:g.9325034A= , CM000681.1:g.9325034A= GRCh37
NC_000019.8:g.9186034A= NCBI36
NG_027953.1:g.5514T=

Transcript Alleles

HGVS Amino-acid change
ENST00000641244.1:c.480T= ENSP00000493404.1:p.Ile160=
ENST00000641669.1:c.480T= MANE Select ENSP00000493383.1:p.Ile160=
ENST00000308682.3:c.480T= ENSP00000310488.2:p.Ile160=
NM_001005191.2:c.480T= NP_001005191.1:p.Ile160=
NM_001005191.3:c.480T= MANE Select NP_001005191.1:p.Ile160=