Product Details

SNP ID

rs745879

Assay Type

Validated

NCBI dbSNP Submissions

30

Location

Chr.1:41479907 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CCTGCTACAATTCTACTCATTCTTC[A/G]AGGTCCAGTTCAAGGTAGTCCAGCC

Phenotype

MIM: 131241

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

EDN2 PubMed Links

Gene Details

Gene

EDN2

Gene Name

endothelin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001302269.1		Intron			NP_001289198.1
NM_001956.4		Intron			NP_001947.1
XM_017000512.1		Intron			XP_016856001.1

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