Canonical Allele Identifier: CA10055999
Gene: LRRC3 HGNC NCBI

Linked Data

dbSNP Id: rs757272139

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456694G>A , CM000683.2:g.44456694G>A GRCh38
NC_000021.8:g.45876577G>A , CM000683.1:g.45876577G>A GRCh37
NC_000021.7:g.44701005G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.50G>A MANE Select ENSP00000291592.4:p.Arg17Gln
ENST00000291592.5:c.50G>A ENSP00000291592.4:p.Arg17Gln
NM_030891.4:c.50G>A NP_112153.1:p.Arg17Gln
NM_030891.5:c.50G>A NP_112153.1:p.Arg17Gln
NM_030891.6:c.50G>A MANE Select NP_112153.1:p.Arg17Gln