Canonical Allele Identifier: CA505453029
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs2050513075
MyVariant Identifiers: chr19:g.9237453G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126777G>T , CM000681.2:g.9126777G>T GRCh38
NC_000019.9:g.9237453G>T , CM000681.1:g.9237453G>T GRCh37
NC_000019.8:g.9098453G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305444.2:c.174C>A MANE Select ENSP00000302867.2:p.Pro58=
NM_001001958.1:c.174C>A MANE Select NP_001001958.1:p.Pro58=