Canonical Allele Identifier: CA2557609205
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274105del , CM000671.2:g.133274105del GRCh38
NC_000009.11:g.136149521del , CM000671.1:g.136149521del GRCh37
NC_000009.10:g.135139342del NCBI36
NG_006669.1:g.3530del
NG_006669.2:g.6110del

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+1057del
ENST00000647353.1:n.53+1057del
ENST00000651471.1:n.63+1857del
ENST00000679909.1:c.28+1057del ENSP00000506089.1:n.28+1057del
ENST00000453660.3:n.40+1057del
ENST00000538324.2:c.28+1057del ENSP00000483018.1:n.28+1057del
ENST00000611156.4:c.28+1057del ENSP00000483265.1:n.28+1057del
NM_020469.2:c.28+1057del NP_065202.2:n.28+1057del
NM_020469.3:c.28+1057del NP_065202.2:n.28+1057del