Canonical Allele Identifier: CA2840263397
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257524del , CM000671.2:g.133257524del GRCh38
NC_000009.11:g.136132911del , CM000671.1:g.136132911del GRCh37
NC_000009.10:g.135122732del NCBI36
NG_006669.1:g.20144del
NG_006669.2:g.22692del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.289del
ENST00000647353.1:n.54-6371del
ENST00000651471.1:n.329+519del
ENST00000679909.1:c.28+17639del ENSP00000506089.1:n.28+17639del
ENST00000453660.3:n.271del
ENST00000538324.2:c.259-2del
ENST00000611156.4:c.259-2del
NM_020469.2:c.259del NP_065202.2:p.Val87Ter
NM_020469.3:c.259del NP_065202.2:p.Val87Ter