Canonical Allele Identifier: CA1410882540
Gene: CLRN1 HGNC NCBI

Linked Data

dbSNP Id: rs1576621908

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150926543T>C , CM000665.2:g.150926543T>C GRCh38
NC_000003.11:g.150644330T>C , CM000665.1:g.150644330T>C GRCh37
NC_000003.10:g.152127020T>C NCBI36
NG_009168.1:g.51457A>G , LRG_700:g.51457A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295911.6:c.*309A>G ENSP00000295911.2:n.*309A>G
ENST00000562308.5:c.104+15039A>G
ENST00000565169.1:c.162+15039A>G
ENST00000569170.5:c.162+15039A>G
NM_052995.2:c.*309A>G , LRG_700t2:c.*309A>G NP_443721.1:n.*309A>G
XR_924167.1:n.2404A>G