Canonical Allele Identifier: CA2786163363
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258397del , CM000671.2:g.133258397del GRCh38
NC_000009.11:g.136133788del , CM000671.1:g.136133788del GRCh37
NC_000009.10:g.135123609del NCBI36
NG_006669.1:g.19267del
NG_006669.2:g.21819del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-264del
ENST00000647353.1:n.54-7244del
ENST00000651471.1:n.239-264del
ENST00000679909.1:c.28+16766del ENSP00000506089.1:n.28+16766del
ENST00000453660.3:n.216-264del
ENST00000538324.2:c.204-264del ENSP00000483018.1:n.204-264del
ENST00000611156.4:c.204-264del ENSP00000483265.1:n.204-264del
NM_020469.2:c.204-264del NP_065202.2:n.204-264del
NM_020469.3:c.204-264del NP_065202.2:n.204-264del