Canonical Allele Identifier: CA1410882519
Gene: CLRN1 HGNC NCBI

Linked Data

dbSNP Id: rs1576621888

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150926506G>A , CM000665.2:g.150926506G>A GRCh38
NC_000003.11:g.150644293G>A , CM000665.1:g.150644293G>A GRCh37
NC_000003.10:g.152126983G>A NCBI36
NG_009168.1:g.51494C>T , LRG_700:g.51494C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295911.6:c.*346C>T ENSP00000295911.2:n.*346C>T
ENST00000562308.5:c.104+15076C>T
ENST00000565169.1:c.162+15076C>T
ENST00000569170.5:c.162+15076C>T
NM_052995.2:c.*346C>T , LRG_700t2:c.*346C>T NP_443721.1:n.*346C>T
XR_924167.1:n.2441C>T