Canonical Allele Identifier: CA410441242
Gene: LRRC3 HGNC NCBI

Linked Data

dbSNP Id: rs1362158061
gnomAD v3: 21-44456855-C-T
gnomAD v4: 21-44456855-C-T
MyVariant Identifiers: chr21:g.45876738C>T (hg19) chr21:g.44456855C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456855C>T , CM000683.2:g.44456855C>T GRCh38
NC_000021.8:g.45876738C>T , CM000683.1:g.45876738C>T GRCh37
NC_000021.7:g.44701166C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.211C>T MANE Select ENSP00000291592.4:p.Leu71Phe
ENST00000291592.5:c.211C>T ENSP00000291592.4:p.Leu71Phe
NM_030891.4:c.211C>T NP_112153.1:p.Leu71Phe
NM_030891.5:c.211C>T NP_112153.1:p.Leu71Phe
NM_030891.6:c.211C>T MANE Select NP_112153.1:p.Leu71Phe
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