Canonical Allele Identifier: CA2321816108
Gene: OR7D4 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000641244.1:c.346G= ENSP00000493404.1:p.Ala116=
ENST00000641669.1:c.346G= MANE Select ENSP00000493383.1:p.Ala116=
ENST00000308682.3:c.346G= ENSP00000310488.2:p.Ala116=
NM_001005191.2:c.346G= NP_001005191.1:p.Ala116=
NM_001005191.3:c.346G= MANE Select NP_001005191.1:p.Ala116=