Canonical Allele Identifier: CA410441442
Gene: LRRC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.45876784A>C (hg19) chr21:g.44456901A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456901A>C , CM000683.2:g.44456901A>C GRCh38
NC_000021.8:g.45876784A>C , CM000683.1:g.45876784A>C GRCh37
NC_000021.7:g.44701212A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.257A>C MANE Select ENSP00000291592.4:p.His86Pro
ENST00000291592.5:c.257A>C ENSP00000291592.4:p.His86Pro
NM_030891.4:c.257A>C NP_112153.1:p.His86Pro
NM_030891.5:c.257A>C NP_112153.1:p.His86Pro
NM_030891.6:c.257A>C MANE Select NP_112153.1:p.His86Pro
Search 100 bp 5'
Search 100 bp 3'