Canonical Allele Identifier: CA10056020
Gene: LRRC3 HGNC NCBI

Linked Data

dbSNP Id: rs367742202
ExAC: 21:45876662 T / C
gnomAD v2: 21-45876662-T-C
gnomAD v3: 21-44456779-T-C
gnomAD v4: 21-44456779-T-C
MyVariant Identifiers: chr21:g.45876662T>C (hg19) chr21:g.44456779T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456779T>C , CM000683.2:g.44456779T>C GRCh38
NC_000021.8:g.45876662T>C , CM000683.1:g.45876662T>C GRCh37
NC_000021.7:g.44701090T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.135T>C MANE Select ENSP00000291592.4:p.Ala45=
ENST00000291592.5:c.135T>C ENSP00000291592.4:p.Ala45=
NM_030891.4:c.135T>C NP_112153.1:p.Ala45=
NM_030891.5:c.135T>C NP_112153.1:p.Ala45=
NM_030891.6:c.135T>C MANE Select NP_112153.1:p.Ala45=
Search 100 bp 5'
Search 100 bp 3'