Canonical Allele Identifier: CA638123128
Gene: LRRC3 HGNC NCBI

Linked Data

dbSNP Id: rs1417629970
gnomAD v2: 21-45876486-C-G
gnomAD v4: 21-44456603-C-G
MyVariant Identifiers: chr21:g.45876486C>G (hg19) chr21:g.44456603C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456603C>G , CM000683.2:g.44456603C>G GRCh38
NC_000021.8:g.45876486C>G , CM000683.1:g.45876486C>G GRCh37
NC_000021.7:g.44700914C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.-42C>G MANE Select ENSP00000291592.4:n.-42C>G
ENST00000291592.5:c.-42C>G ENSP00000291592.4:n.-42C>G
NM_030891.4:c.-42C>G NP_112153.1:n.-42C>G
NM_030891.5:c.-42C>G NP_112153.1:n.-42C>G
NM_030891.6:c.-42C>G MANE Select NP_112153.1:n.-42C>G
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