Canonical Allele Identifier: CA2786162918
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255428_133255507del , CM000671.2:g.133255428_133255507del GRCh38
NC_000009.11:g.136130815_136130894del , CM000671.1:g.136130815_136130894del GRCh37
NC_000009.10:g.135120636_135120715del NCBI36
NG_006669.1:g.22162_22241del
NG_006669.2:g.24710_24789del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1254_1333del
ENST00000647353.1:n.54-4354_54-4275del
ENST00000679909.1:c.28+19656_28+19735del ENSP00000506089.1:n.28+19656_28+19735del
ENST00000453660.3:n.1236_1315del
ENST00000611156.4:c.*160_*239del ENSP00000483265.1:n.*160_*239del
NM_020469.2:c.*160_*239del NP_065202.2:n.*160_*239del
NM_020469.3:c.*160_*239del NP_065202.2:n.*160_*239del