Canonical Allele Identifier: CA1882578604
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255390_133255400delinsTTCTGTGTGTG , CM000671.2:g.133255390_133255400delinsTTCTGTGTGTG GRCh38
NC_000009.11:g.136130777_136130787delinsTTCTGTGTGTG , CM000671.1:g.136130777_136130787delinsTTCTGTGTGTG GRCh37
NC_000009.10:g.135120598_135120608delinsTTCTGTGTGTG NCBI36
NG_006669.1:g.22268_22278delinsCACACACAGAA
NG_006669.2:g.24816_24826delinsCACACACAGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1360_1370delinsCACACACAGAA
ENST00000647353.1:n.54-4248_54-4238delinsCACACACAGAA
ENST00000679909.1:c.28+19762_28+19772delinsCACACACAGAA ENSP00000506089.1:n.28+19762_28+19772delinsCACACACAGAA
ENST00000453660.3:n.1342_1352delinsCACACACAGAA
ENST00000611156.4:c.*266_*276delinsCACACACAGAA ENSP00000483265.1:n.*266_*276delinsCACACACAGAA
NM_020469.2:c.*266_*276delinsCACACACAGAA NP_065202.2:n.*266_*276delinsCACACACAGAA
NM_020469.3:c.*266_*276delinsCACACACAGAA NP_065202.2:n.*266_*276delinsCACACACAGAA