Canonical Allele Identifier: CA2692330307
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255392_133255395del , CM000671.2:g.133255392_133255395del GRCh38
NC_000009.11:g.136130779_136130782del , CM000671.1:g.136130779_136130782del GRCh37
NC_000009.10:g.135120600_135120603del NCBI36
NG_006669.1:g.22274_22277del
NG_006669.2:g.24822_24825del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1366_1369del
ENST00000647353.1:n.54-4242_54-4239del
ENST00000679909.1:c.28+19768_28+19771del ENSP00000506089.1:n.28+19768_28+19771del
ENST00000453660.3:n.1348_1351del
ENST00000611156.4:c.*272_*275del ENSP00000483265.1:n.*272_*275del
NM_020469.2:c.*272_*275del NP_065202.2:n.*272_*275del
NM_020469.3:c.*272_*275del NP_065202.2:n.*272_*275del