Canonical Allele Identifier: CA2692330332
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255511del , CM000671.2:g.133255511del GRCh38
NC_000009.11:g.136130898del , CM000671.1:g.136130898del GRCh37
NC_000009.10:g.135120719del NCBI36
NG_006669.1:g.22157del
NG_006669.2:g.24705del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1249del
ENST00000647353.1:n.54-4359del
ENST00000679909.1:c.28+19651del ENSP00000506089.1:n.28+19651del
ENST00000453660.3:n.1231del
ENST00000611156.4:c.*155del ENSP00000483265.1:n.*155del
NM_020469.2:c.*155del NP_065202.2:n.*155del
NM_020469.3:c.*155del NP_065202.2:n.*155del