Canonical Allele Identifier: CA10056006
Gene: LRRC3 HGNC NCBI

Linked Data

dbSNP Id: rs749506974
ExAC: 21:45876617 C / T
gnomAD v2: 21-45876617-C-T
gnomAD v4: 21-44456734-C-T
MyVariant Identifiers: chr21:g.45876617C>T (hg19) chr21:g.44456734C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456734C>T , CM000683.2:g.44456734C>T GRCh38
NC_000021.8:g.45876617C>T , CM000683.1:g.45876617C>T GRCh37
NC_000021.7:g.44701045C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.90C>T MANE Select ENSP00000291592.4:p.Gly30=
ENST00000291592.5:c.90C>T ENSP00000291592.4:p.Gly30=
NM_030891.4:c.90C>T NP_112153.1:p.Gly30=
NM_030891.5:c.90C>T NP_112153.1:p.Gly30=
NM_030891.6:c.90C>T MANE Select NP_112153.1:p.Gly30=
Search 100 bp 5'
Search 100 bp 3'