Product Details

SNP ID

hCV89709212

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:144114690 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAACTGCAAATATTAACACCAACC[G/T]GGATTTTCTATTTCAACAGAACTTA

Phenotype

MIM: 111300

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

GYPA PubMed Links

Gene Details

Gene

GYPA

Gene Name

glycophorin A (MNS blood group)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001308187.1	547	Silent Mutation	CCA,CCC	P132P	NP_001295116.1
NM_001308190.1	547	Silent Mutation	CCA,CCC	P112P	NP_001295119.1
NM_002099.7	547	Silent Mutation	CCA,CCC	P145P	NP_002090.4

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