Canonical Allele Identifier: CA410440245
Gene: LRRC3 HGNC NCBI

Linked Data

dbSNP Id: rs1601288372
gnomAD v4: 21-44456690-A-C
MyVariant Identifiers: chr21:g.45876573A>C (hg19) chr21:g.44456690A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456690A>C , CM000683.2:g.44456690A>C GRCh38
NC_000021.8:g.45876573A>C , CM000683.1:g.45876573A>C GRCh37
NC_000021.7:g.44701001A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.46A>C MANE Select ENSP00000291592.4:p.Thr16Pro
ENST00000291592.5:c.46A>C ENSP00000291592.4:p.Thr16Pro
NM_030891.4:c.46A>C NP_112153.1:p.Thr16Pro
NM_030891.5:c.46A>C NP_112153.1:p.Thr16Pro
NM_030891.6:c.46A>C MANE Select NP_112153.1:p.Thr16Pro
Search 100 bp 5'
Search 100 bp 3'