Canonical Allele Identifier: CA410441465
Gene: LRRC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.45876789C>T (hg19) chr21:g.44456906C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456906C>T , CM000683.2:g.44456906C>T GRCh38
NC_000021.8:g.45876789C>T , CM000683.1:g.45876789C>T GRCh37
NC_000021.7:g.44701217C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.262C>T MANE Select ENSP00000291592.4:p.His88Tyr
ENST00000291592.5:c.262C>T ENSP00000291592.4:p.His88Tyr
NM_030891.4:c.262C>T NP_112153.1:p.His88Tyr
NM_030891.5:c.262C>T NP_112153.1:p.His88Tyr
NM_030891.6:c.262C>T MANE Select NP_112153.1:p.His88Tyr
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Search 100 bp 3'