Canonical Allele Identifier: CA512671935
Gene: LRRC3 HGNC NCBI

Linked Data

dbSNP Id: rs201964764
MyVariant Identifiers: chr21:g.45876792C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456909C>A , CM000683.2:g.44456909C>A GRCh38
NC_000021.8:g.45876792C>A , CM000683.1:g.45876792C>A GRCh37
NC_000021.7:g.44701220C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.265C>A MANE Select ENSP00000291592.4:p.Arg89=
ENST00000291592.5:c.265C>A ENSP00000291592.4:p.Arg89=
NM_030891.4:c.265C>A NP_112153.1:p.Arg89=
NM_030891.5:c.265C>A NP_112153.1:p.Arg89=
NM_030891.6:c.265C>A MANE Select NP_112153.1:p.Arg89=