Canonical Allele Identifier: CA410440749
Gene: LRRC3 HGNC NCBI

Linked Data

gnomAD v4: 21-44456747-C-A
MyVariant Identifiers: chr21:g.45876630C>A (hg19) chr21:g.44456747C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456747C>A , CM000683.2:g.44456747C>A GRCh38
NC_000021.8:g.45876630C>A , CM000683.1:g.45876630C>A GRCh37
NC_000021.7:g.44701058C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000291592.6:c.103C>A MANE Select ENSP00000291592.4:p.Gln35Lys
ENST00000291592.5:c.103C>A ENSP00000291592.4:p.Gln35Lys
NM_030891.4:c.103C>A NP_112153.1:p.Gln35Lys
NM_030891.5:c.103C>A NP_112153.1:p.Gln35Lys
NM_030891.6:c.103C>A MANE Select NP_112153.1:p.Gln35Lys
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