Canonical Allele Identifier: CA2539418785
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260185_133260199del , CM000671.2:g.133260185_133260199del GRCh38
NC_000009.11:g.136135589_136135603del , CM000671.1:g.136135589_136135603del GRCh37
NC_000009.10:g.135125410_135125424del NCBI36
NG_006669.1:g.17455_17469del
NG_006669.2:g.20020_20034del

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.186-329_186-315del
ENST00000647353.1:n.54-9043_54-9029del
ENST00000651471.1:n.191-329_191-315del
ENST00000679909.1:c.28+14967_28+14981del ENSP00000506089.1:n.28+14967_28+14981del
ENST00000453660.3:n.168-329_168-315del
ENST00000538324.2:c.156-329_156-315del ENSP00000483018.1:n.156-329_156-315del
ENST00000611156.4:c.156-329_156-315del ENSP00000483265.1:n.156-329_156-315del
NM_020469.2:c.156-329_156-315del NP_065202.2:n.156-329_156-315del
NM_020469.3:c.156-329_156-315del NP_065202.2:n.156-329_156-315del