Canonical Allele Identifier: CA243636067
Gene: CRY1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11113179

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.107059007C>T , CM000674.2:g.107059007C>T GRCh38
NC_000012.10:g.105976915C>T NCBI36
NC_000012.11:g.107452785C>T , CM000674.1:g.107452785C>T GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000008527.9:c.158+33797G>A ENSP00000008527.5:p.=
NM_004075.4:c.158+33797G>A VV NP_004066.1:p.=
XM_011537939.1:c.74+13928G>A XP_011536241.1:p.=