Canonical Allele Identifier: CA512518361
Gene: LRRC3 HGNC NCBI

Linked Data

gnomAD v4: 21-44456656-G-T
MyVariant Identifiers: chr21:g.45876539G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456656G>T , CM000683.2:g.44456656G>T GRCh38
NC_000021.8:g.45876539G>T , CM000683.1:g.45876539G>T GRCh37
NC_000021.7:g.44700967G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.12G>T MANE Select ENSP00000291592.4:p.Val4=
ENST00000291592.5:c.12G>T ENSP00000291592.4:p.Val4=
NM_030891.4:c.12G>T NP_112153.1:p.Val4=
NM_030891.5:c.12G>T NP_112153.1:p.Val4=
NM_030891.6:c.12G>T MANE Select NP_112153.1:p.Val4=
Search 100 bp 5'
Search 100 bp 3'