Canonical Allele Identifier: CA10056013
Gene: LRRC3 HGNC NCBI

Linked Data

dbSNP Id: rs761007262
ExAC: 21:45876640 G / C
gnomAD v4: 21-44456757-G-C
MyVariant Identifiers: chr21:g.45876640G>C (hg19) chr21:g.44456757G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456757G>C , CM000683.2:g.44456757G>C GRCh38
NC_000021.8:g.45876640G>C , CM000683.1:g.45876640G>C GRCh37
NC_000021.7:g.44701068G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.113G>C MANE Select ENSP00000291592.4:p.Arg38Pro
ENST00000291592.5:c.113G>C ENSP00000291592.4:p.Arg38Pro
NM_030891.4:c.113G>C NP_112153.1:p.Arg38Pro
NM_030891.5:c.113G>C NP_112153.1:p.Arg38Pro
NM_030891.6:c.113G>C MANE Select NP_112153.1:p.Arg38Pro
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