Canonical Allele Identifier: CA410440760
Gene: LRRC3 HGNC NCBI

Linked Data

dbSNP Id: rs2051703990
gnomAD v3: 21-44456750-C-T
gnomAD v4: 21-44456750-C-T
MyVariant Identifiers: chr21:g.45876633C>T (hg19) chr21:g.44456750C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456750C>T , CM000683.2:g.44456750C>T GRCh38
NC_000021.8:g.45876633C>T , CM000683.1:g.45876633C>T GRCh37
NC_000021.7:g.44701061C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.106C>T MANE Select ENSP00000291592.4:p.Pro36Ser
ENST00000291592.5:c.106C>T ENSP00000291592.4:p.Pro36Ser
NM_030891.4:c.106C>T NP_112153.1:p.Pro36Ser
NM_030891.5:c.106C>T NP_112153.1:p.Pro36Ser
NM_030891.6:c.106C>T MANE Select NP_112153.1:p.Pro36Ser
Search 100 bp 5'
Search 100 bp 3'