Product Details

SNP ID

rs2292913

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:45855978 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CACTAACAAGGCCTGTGTGGACTCC[A/G]CAGGTTCCTACTTCAGTCTCTGGAA

Phenotype

MIM: 603732

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CRY2 PubMed Links

Gene Details

Gene

CRY2

Gene Name

cryptochrome circadian clock 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001127457.2		Intron			NP_001120929.1
NM_021117.3		Intron			NP_066940.2

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