Canonical Allele Identifier: CA10055978

Gene: LRRC3

Linked Data

• dbSNP Id: rs777743109
• ExAC: 21:45876499 G / C
• gnomAD v2: 21-45876499-G-C
• gnomAD v3: 21-44456616-G-C
• gnomAD v4: 21-44456616-G-C
• MyVariant Identifiers: chr21:g.45876499G>C (hg19) ; chr21:g.44456616G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44456616G>C , CM000683.2:g.44456616G>C	GRCh38
NC_000021.8:g.45876499G>C , CM000683.1:g.45876499G>C	GRCh37
NC_000021.7:g.44700927G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291592.6:c.-29G>C MANE Select	ENSP00000291592.4:n.-29G>C
ENST00000291592.5:c.-29G>C	ENSP00000291592.4:n.-29G>C
NM_030891.4:c.-29G>C	NP_112153.1:n.-29G>C
NM_030891.5:c.-29G>C	NP_112153.1:n.-29G>C
NM_030891.6:c.-29G>C MANE Select	NP_112153.1:n.-29G>C