Canonical Allele Identifier: CA1882578312
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255280_133255334delinsAATGGTGTGTTTCTGTGGCCGGAAGGGCGTATCTGCGATTGCGTGTCTGTGTATG , CM000671.2:g.133255280_133255334delinsAATGGTGTGTTTCTGTGGCCGGAAGGGCGTATCTGCGATTGCGTGTCTGTGTATG GRCh38
NC_000009.11:g.136130667_136130721delinsAATGGTGTGTTTCTGTGGCCGGAAGGGCGTATCTGCGATTGCGTGTCTGTGTATG , CM000671.1:g.136130667_136130721delinsAATGGTGTGTTTCTGTGGCCGGAAGGGCGTATCTGCGATTGCGTGTCTGTGTATG GRCh37
NC_000009.10:g.135120488_135120542delinsAATGGTGTGTTTCTGTGGCCGGAAGGGCGTATCTGCGATTGCGTGTCTGTGTATG NCBI36
NG_006669.1:g.22334_22388delinsCATACACAGACACGCAATCGCAGATACGCCCTTCCGGCCACAGAAACACACCATT
NG_006669.2:g.24882_24936delinsCATACACAGACACGCAATCGCAGATACGCCCTTCCGGCCACAGAAACACACCATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1426_1480delinsCATACACAGACACGCAATCGCAGATACGCCCTTCCGGCCACAGAAACACACCATT
ENST00000647353.1:n.54-4182_54-4128delinsCATACACAGACACGCAATCGCAGATACGCCCTTCCGGCCACAGAAACACACCATT
ENST00000679909.1:c.28+19828_28+19882delinsCATACACAGACACGCAATCGCAGATACGCCCTTCCGGCCACAGAAACACACCATT ENSP00000506089.1:n.28+19828_28+19882delinsCATACACAGACACGCAAT...
ENST00000453660.3:n.1408_1462delinsCATACACAGACACGCAATCGCAGATACGCCCTTCCGGCCACAGAAACACACCATT
ENST00000611156.4:c.*332_*386delinsCATACACAGACACGCAATCGCAGATACGCCCTTCCGGCCACAGAAACACACCATT ENSP00000483265.1:n.*332_*386delinsCATACACAGACACGCAATCGCAGATA...
NM_020469.2:c.*332_*386delinsCATACACAGACACGCAATCGCAGATACGCCCTTCCGGCCACAGAAACACACCATT NP_065202.2:n.*332_*386delinsCATACACAGACACGCAATCGCAGATACGCCCT...
NM_020469.3:c.*332_*386delinsCATACACAGACACGCAATCGCAGATACGCCCTTCCGGCCACAGAAACACACCATT NP_065202.2:n.*332_*386delinsCATACACAGACACGCAATCGCAGATACGCCCT...