Canonical Allele Identifier: CA2692330304
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255377_133255528del , CM000671.2:g.133255377_133255528del GRCh38
NC_000009.11:g.136130764_136130915del , CM000671.1:g.136130764_136130915del GRCh37
NC_000009.10:g.135120585_135120736del NCBI36
NG_006669.1:g.22153_22304del
NG_006669.2:g.24701_24852del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1245_1396del
ENST00000647353.1:n.54-4363_54-4212del
ENST00000679909.1:c.28+19647_28+19798del ENSP00000506089.1:n.28+19647_28+19798del
ENST00000453660.3:n.1227_1378del
ENST00000611156.4:c.*151_*302del ENSP00000483265.1:n.*151_*302del
NM_020469.2:c.*151_*302del NP_065202.2:n.*151_*302del
NM_020469.3:c.*151_*302del NP_065202.2:n.*151_*302del