Canonical Allele Identifier: CA512518378
Gene: LRRC3 HGNC NCBI

Linked Data

dbSNP Id: rs1353513129
gnomAD v2: 21-45876557-G-A
gnomAD v4: 21-44456674-G-A
MyVariant Identifiers: chr21:g.45876557G>A (hg19) chr21:g.44456674G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456674G>A , CM000683.2:g.44456674G>A GRCh38
NC_000021.8:g.45876557G>A , CM000683.1:g.45876557G>A GRCh37
NC_000021.7:g.44700985G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.30G>A MANE Select ENSP00000291592.4:p.Ser10=
ENST00000291592.5:c.30G>A ENSP00000291592.4:p.Ser10=
NM_030891.4:c.30G>A NP_112153.1:p.Ser10=
NM_030891.5:c.30G>A NP_112153.1:p.Ser10=
NM_030891.6:c.30G>A MANE Select NP_112153.1:p.Ser10=
Search 100 bp 5'
Search 100 bp 3'