Canonical Allele Identifier: CA2692330309
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255433_133255434del , CM000671.2:g.133255433_133255434del GRCh38
NC_000009.11:g.136130820_136130821del , CM000671.1:g.136130820_136130821del GRCh37
NC_000009.10:g.135120641_135120642del NCBI36
NG_006669.1:g.22235_22236del
NG_006669.2:g.24783_24784del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1327_1328del
ENST00000647353.1:n.54-4281_54-4280del
ENST00000679909.1:c.28+19729_28+19730del ENSP00000506089.1:n.28+19729_28+19730del
ENST00000453660.3:n.1309_1310del
ENST00000611156.4:c.*233_*234del ENSP00000483265.1:n.*233_*234del
NM_020469.2:c.*233_*234del NP_065202.2:n.*233_*234del
NM_020469.3:c.*233_*234del NP_065202.2:n.*233_*234del