Canonical Allele Identifier: CA2692330662
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257662_133257663del , CM000671.2:g.133257662_133257663del GRCh38
NC_000009.11:g.136133049_136133050del , CM000671.1:g.136133049_136133050del GRCh37
NC_000009.10:g.135122870_135122871del NCBI36
NG_006669.1:g.20005_20006del
NG_006669.2:g.22553_22554del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-120_270-119del
ENST00000647353.1:n.54-6510_54-6509del
ENST00000651471.1:n.329+380_329+381del
ENST00000679909.1:c.28+17500_28+17501del ENSP00000506089.1:n.28+17500_28+17501del
ENST00000453660.3:n.252-120_252-119del
ENST00000538324.2:c.240-120_240-119del ENSP00000483018.1:n.240-120_240-119del
ENST00000611156.4:c.240-120_240-119del ENSP00000483265.1:n.240-120_240-119del
NM_020469.2:c.240-120_240-119del NP_065202.2:n.240-120_240-119del
NM_020469.3:c.240-120_240-119del NP_065202.2:n.240-120_240-119del