Canonical Allele Identifier: CA2692331584
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133262045_133262047del , CM000671.2:g.133262045_133262047del GRCh38
NC_000009.11:g.136137448_136137450del , CM000671.1:g.136137448_136137450del GRCh37
NC_000009.10:g.135127269_135127271del NCBI36
NG_006669.1:g.15606_15608del
NG_006669.2:g.18172_18174del

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.128+56_128+58del
ENST00000647353.1:n.54-10891_54-10889del
ENST00000651471.1:n.133+56_133+58del
ENST00000679909.1:c.28+13119_28+13121del ENSP00000506089.1:n.28+13119_28+13121del
ENST00000453660.3:n.110+56_110+58del
ENST00000538324.2:c.98+56_98+58del ENSP00000483018.1:n.98+56_98+58del
ENST00000611156.4:c.98+56_98+58del ENSP00000483265.1:n.98+56_98+58del
NM_020469.2:c.98+56_98+58del NP_065202.2:n.98+56_98+58del
NM_020469.3:c.98+56_98+58del NP_065202.2:n.98+56_98+58del