Canonical Allele Identifier: CA1129724773
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274125_133274127del , CM000671.2:g.133274125_133274127del GRCh38
NC_000009.11:g.136149541_136149543del , CM000671.1:g.136149541_136149543del GRCh37
NC_000009.10:g.135139362_135139364del NCBI36
NG_006669.1:g.3508_3510del
NG_006669.2:g.6088_6090del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.58+1035_58+1037del
ENST00000647353.1:n.53+1035_53+1037del
ENST00000651471.1:n.63+1835_63+1837del
ENST00000679909.1:c.28+1035_28+1037del ENSP00000506089.1:n.28+1035_28+1037del
ENST00000453660.3:n.40+1035_40+1037del
ENST00000538324.2:c.28+1035_28+1037del ENSP00000483018.1:n.28+1035_28+1037del
ENST00000611156.4:c.28+1035_28+1037del ENSP00000483265.1:n.28+1035_28+1037del
NM_020469.2:c.28+1035_28+1037del NP_065202.2:n.28+1035_28+1037del
NM_020469.3:c.28+1035_28+1037del NP_065202.2:n.28+1035_28+1037del