Canonical Allele Identifier: CA410440282
Gene: LRRC3 HGNC NCBI

Linked Data

dbSNP Id: rs757272139
gnomAD v2: 21-45876577-G-C
gnomAD v4: 21-44456694-G-C
MyVariant Identifiers: chr21:g.45876577G>C (hg19) chr21:g.44456694G>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.50G>C MANE Select ENSP00000291592.4:p.Arg17Pro
ENST00000291592.5:c.50G>C ENSP00000291592.4:p.Arg17Pro
NM_030891.4:c.50G>C NP_112153.1:p.Arg17Pro
NM_030891.5:c.50G>C NP_112153.1:p.Arg17Pro
NM_030891.6:c.50G>C MANE Select NP_112153.1:p.Arg17Pro
Search 100 bp 5'
Search 100 bp 3'