Canonical Allele Identifier: CA410440235
Gene: LRRC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.45876571C>A (hg19) chr21:g.44456688C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456688C>A , CM000683.2:g.44456688C>A GRCh38
NC_000021.8:g.45876571C>A , CM000683.1:g.45876571C>A GRCh37
NC_000021.7:g.44700999C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.44C>A MANE Select ENSP00000291592.4:p.Ser15Tyr
ENST00000291592.5:c.44C>A ENSP00000291592.4:p.Ser15Tyr
NM_030891.4:c.44C>A NP_112153.1:p.Ser15Tyr
NM_030891.5:c.44C>A NP_112153.1:p.Ser15Tyr
NM_030891.6:c.44C>A MANE Select NP_112153.1:p.Ser15Tyr
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