Product Details

SNP ID

rs143190420

Assay Type

Functionally tested

NCBI dbSNP Submissions

11

Location

Chr.1:207455728 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACACTTTTTCTAAGAGCAGAGTAC[A/G]TCCCTGACTTCTCACCTATTTCTAA

Phenotype

MIM: 120650

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CR2 PubMed Links

Gene Details

Gene

CR2

Gene Name

complement component 3d receptor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001006658.2		Intron			NP_001006659.1
NM_001877.4		Intron			NP_001868.2
XM_011509206.2		Intron			XP_011507508.1

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