Canonical Allele Identifier: CA10056032
Gene: LRRC3 HGNC NCBI

Linked Data

dbSNP Id: rs116969723

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456833G>A , CM000683.2:g.44456833G>A GRCh38
NC_000021.8:g.45876716G>A , CM000683.1:g.45876716G>A GRCh37
NC_000021.7:g.44701144G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000291592.6:c.189G>A MANE Select ENSP00000291592.4:p.Pro63=
ENST00000291592.5:c.189G>A ENSP00000291592.4:p.Pro63=
NM_030891.4:c.189G>A NP_112153.1:p.Pro63=
NM_030891.5:c.189G>A NP_112153.1:p.Pro63=
NM_030891.6:c.189G>A MANE Select NP_112153.1:p.Pro63=