Canonical Allele Identifier: CA9175425
Gene: OR7D4 HGNC NCBI

Linked Data

dbSNP Id: rs750669605
ExAC: 19:9325160 C / T
gnomAD v2: 19-9325160-C-T
gnomAD v3: 19-9214484-C-T
gnomAD v4: 19-9214484-C-T
MyVariant Identifiers: chr19:g.9325160C>T (hg19) chr19:g.9214484C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9214484C>T , CM000681.2:g.9214484C>T GRCh38
NC_000019.9:g.9325160C>T , CM000681.1:g.9325160C>T GRCh37
NC_000019.8:g.9186160C>T NCBI36
NG_027953.1:g.5388G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000641244.1:c.354G>A ENSP00000493404.1:p.Met118Ile
ENST00000641669.1:c.354G>A MANE Select ENSP00000493383.1:p.Met118Ile
ENST00000308682.3:c.354G>A ENSP00000310488.2:p.Met118Ile
NM_001005191.2:c.354G>A NP_001005191.1:p.Met118Ile
NM_001005191.3:c.354G>A MANE Select NP_001005191.1:p.Met118Ile
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