Canonical Allele Identifier: CA1882590641
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274293_133274294delinsAC , CM000671.2:g.133274293_133274294delinsAC GRCh38
NC_000009.11:g.136149709_136149710delinsAC , CM000671.1:g.136149709_136149710delinsAC GRCh37
NC_000009.10:g.135139530_135139531delinsAC NCBI36
NG_006669.1:g.3341_3342delinsGT
NG_006669.2:g.5921_5922delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+868_58+869delinsGT
ENST00000647353.1:n.53+868_53+869delinsGT
ENST00000651471.1:n.63+1668_63+1669delinsGT
ENST00000679909.1:c.28+868_28+869delinsGT ENSP00000506089.1:n.28+868_28+869delinsGT...
ENST00000453660.3:n.40+868_40+869delinsGT
ENST00000538324.2:c.28+868_28+869delinsGT ENSP00000483018.1:n.28+868_28+869delinsGT...
ENST00000611156.4:c.28+868_28+869delinsGT ENSP00000483265.1:n.28+868_28+869delinsGT...
NM_020469.2:c.28+868_28+869delinsGT NP_065202.2:n.28+868_28+869delinsGT
NM_020469.3:c.28+868_28+869delinsGT NP_065202.2:n.28+868_28+869delinsGT