Canonical Allele Identifier: CA1882578638

Gene: ABO

Linked Data

• dbSNP Id: rs1834547650

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255395_133255396insATGTCT , CM000671.2:g.133255395_133255396insATGTCT	GRCh38
NC_000009.11:g.136130782_136130783insATGTCT , CM000671.1:g.136130782_136130783insATGTCT	GRCh37
NC_000009.10:g.135120603_135120604insATGTCT	NCBI36
NG_006669.1:g.22273_22274insGACATA
NG_006669.2:g.24821_24822insGACATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1365_1366insGACATA
ENST00000647353.1:n.54-4243_54-4242insGACATA
ENST00000679909.1:c.28+19767_28+19768insGACATA	ENSP00000506089.1:n.28+19767_28+19768insGACATA
ENST00000453660.3:n.1347_1348insGACATA
ENST00000611156.4:c.*271_*272insGACATA	ENSP00000483265.1:n.*271_*272insGACATA
NM_020469.2:c.*271_*272insGACATA	NP_065202.2:n.*271_*272insGACATA
NM_020469.3:c.*271_*272insGACATA	NP_065202.2:n.*271_*272insGACATA