Canonical Allele Identifier: CA321807040
Gene: LRRC3 HGNC NCBI

Linked Data

dbSNP Id: rs868195717
gnomAD v4: 21-44456719-C-T
MyVariant Identifiers: chr21:g.45876602C>T (hg19) chr21:g.44456719C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456719C>T , CM000683.2:g.44456719C>T GRCh38
NC_000021.8:g.45876602C>T , CM000683.1:g.45876602C>T GRCh37
NC_000021.7:g.44701030C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.75C>T MANE Select ENSP00000291592.4:p.Phe25=
ENST00000291592.5:c.75C>T ENSP00000291592.4:p.Phe25=
NM_030891.4:c.75C>T NP_112153.1:p.Phe25=
NM_030891.5:c.75C>T NP_112153.1:p.Phe25=
NM_030891.6:c.75C>T MANE Select NP_112153.1:p.Phe25=
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