Canonical Allele Identifier: CA410441171
Gene: LRRC3 HGNC NCBI

Linked Data

dbSNP Id: rs2051705388
gnomAD v3: 21-44456826-A-T
gnomAD v4: 21-44456826-A-T
MyVariant Identifiers: chr21:g.45876709A>T (hg19) chr21:g.44456826A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456826A>T , CM000683.2:g.44456826A>T GRCh38
NC_000021.8:g.45876709A>T , CM000683.1:g.45876709A>T GRCh37
NC_000021.7:g.44701137A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.182A>T MANE Select ENSP00000291592.4:p.Asp61Val
ENST00000291592.5:c.182A>T ENSP00000291592.4:p.Asp61Val
NM_030891.4:c.182A>T NP_112153.1:p.Asp61Val
NM_030891.5:c.182A>T NP_112153.1:p.Asp61Val
NM_030891.6:c.182A>T MANE Select NP_112153.1:p.Asp61Val
Search 100 bp 5'
Search 100 bp 3'