Canonical Allele Identifier: CA321807074
Gene: LRRC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2302318
ClinVar RCV Id: RCV004148452
dbSNP Id: rs142928276
gnomAD v2: 21-45876639-C-G
gnomAD v3: 21-44456756-C-G
gnomAD v4: 21-44456756-C-G
MyVariant Identifiers: chr21:g.45876639C>G (hg19) chr21:g.44456756C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456756C>G , CM000683.2:g.44456756C>G GRCh38
NC_000021.8:g.45876639C>G , CM000683.1:g.45876639C>G GRCh37
NC_000021.7:g.44701067C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.112C>G MANE Select ENSP00000291592.4:p.Arg38Gly
ENST00000291592.5:c.112C>G ENSP00000291592.4:p.Arg38Gly
NM_030891.4:c.112C>G NP_112153.1:p.Arg38Gly
NM_030891.5:c.112C>G NP_112153.1:p.Arg38Gly
NM_030891.6:c.112C>G MANE Select NP_112153.1:p.Arg38Gly
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