Canonical Allele Identifier: CA410441369
Gene: LRRC3 HGNC NCBI

Linked Data

COSMIC: COSM373645
MyVariant Identifiers: chr21:g.45876768G>T (hg19) chr21:g.44456885G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456885G>T , CM000683.2:g.44456885G>T GRCh38
NC_000021.8:g.45876768G>T , CM000683.1:g.45876768G>T GRCh37
NC_000021.7:g.44701196G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.241G>T MANE Select ENSP00000291592.4:p.Asp81Tyr
ENST00000291592.5:c.241G>T ENSP00000291592.4:p.Asp81Tyr
NM_030891.4:c.241G>T NP_112153.1:p.Asp81Tyr
NM_030891.5:c.241G>T NP_112153.1:p.Asp81Tyr
NM_030891.6:c.241G>T MANE Select NP_112153.1:p.Asp81Tyr
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