Canonical Allele Identifier: CA467853009

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131238_136131239insCCGATGACGAAGACGATGACGGCGAGGAATCCGACGGTGAGGTCGGTGGGGAAGCCGGTGCGTTGCACCGCGGCTATGAAACGGTTGGAACTGGGCATCGGA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255851_133255852insCCGATGACGAAGACGATGACGGCGAGGAATCCGACGGTGAGGTCGGTGGGGAAGCCGGTGCGTTGCACCGCGGCTATGAAACGGTTGGAACTGGGCATCGGA , CM000671.2:g.133255851_133255852insCCGATGACGAAGACGATGACGGCGAGGAATCCGACGGTGAGGTCGGTGGGGAAGCCGGTGCGTTGCACCGCGGCTATGAAACGGTTGGAACTGGGCATCGGA	GRCh38
NC_000009.11:g.136131238_136131239insCCGATGACGAAGACGATGACGGCGAGGAATCCGACGGTGAGGTCGGTGGGGAAGCCGGTGCGTTGCACCGCGGCTATGAAACGGTTGGAACTGGGCATCGGA , CM000671.1:g.136131238_136131239insCCGATGACGAAGACGATGACGGCGAGGAATCCGACGGTGAGGTCGGTGGGGAAGCCGGTGCGTTGCACCGCGGCTATGAAACGGTTGGAACTGGGCATCGGA	GRCh37
NC_000009.10:g.135121059_135121060insCCGATGACGAAGACGATGACGGCGAGGAATCCGACGGTGAGGTCGGTGGGGAAGCCGGTGCGTTGCACCGCGGCTATGAAACGGTTGGAACTGGGCATCGGA	NCBI36
NG_006669.1:g.21816_21817insTCCGATGCCCAGTTCCAACCGTTTCATAGCCGCGGTGCAACGCACCGGCTTCCCCACCGACCTCACCGTCGGATTCCTCGCCGTCATCGTCTTCGTCATCGG
NG_006669.2:g.24364_24365insTCCGATGCCCAGTTCCAACCGTTTCATAGCCGCGGTGCAACGCACCGGCTTCCCCACCGACCTCACCGTCGGATTCCTCGCCGTCATCGTCTTCGTCATCGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.908_909insTCCGATGCCCAGTTCCAACCGTTTCATAGCCGCGGTGCAACGCACCGGCTTCCCCACCGACCTCACCGTCGGATTCCTCGCCGTCATCGTCTTCGTCATCGG
ENST00000647353.1:n.54-4700_54-4699insTCCGATGCCCAGTTCCAACCGTTTCATAGCCGCGGTGCAACGCACCGGCTTCCCCACCGACCTCACCGTCGGATTCCTCGCCGTCATCGTCTTCGTCATCGG
ENST00000679909.1:c.28+19310_28+19311insTCCGATGCCCAGTTCCAACCGTTTCATAGCCGCGGTGCAACGCACCGGCTTCCCCACCGACCTCACCGTCGGATTCCTCGCCGTCATCGTCTTCGTCATCGG	ENSP00000506089.1:n.28+19310_28+19311insTCCGATGCCCAGTTCCAACCG...
ENST00000453660.3:n.890_891insTCCGATGCCCAGTTCCAACCGTTTCATAGCCGCGGTGCAACGCACCGGCTTCCCCACCGACCTCACCGTCGGATTCCTCGCCGTCATCGTCTTCGTCATCGG
ENST00000538324.2:c.876_877insTCCGATGCCCAGTTCCAACCGTTTCATAGCCGCGGTGCAACGCACCGGCTTCCCCACCGACCTCACCGTCGGATTCCTCGCCGTCATCGTCTTCGTCATCGG	ENSP00000483018.1:p.Ala292_Asn293insSerAspAlaGlnPheGlnProPheH...
ENST00000611156.4:c.876_877insTCCGATGCCCAGTTCCAACCGTTTCATAGCCGCGGTGCAACGCACCGGCTTCCCCACCGACCTCACCGTCGGATTCCTCGCCGTCATCGTCTTCGTCATCGG	ENSP00000483265.1:p.Ala292_Asn293insSerAspAlaGlnPheGlnProPheH...
NM_020469.2:c.879_880insTCCGATGCCCAGTTCCAACCGTTTCATAGCCGCGGTGCAACGCACCGGCTTCCCCACCGACCTCACCGTCGGATTCCTCGCCGTCATCGTCTTCGTCATCGG	NP_065202.2:p.Ala293_Asn294insSerAspAlaGlnPheGlnProPheHisSerA...
NM_020469.3:c.879_880insTCCGATGCCCAGTTCCAACCGTTTCATAGCCGCGGTGCAACGCACCGGCTTCCCCACCGACCTCACCGTCGGATTCCTCGCCGTCATCGTCTTCGTCATCGG	NP_065202.2:p.Ala293_Asn294insSerAspAlaGlnPheGlnProPheHisSerA...