Canonical Allele Identifier: CA1882590642
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274293_133274295delinsACA , CM000671.2:g.133274293_133274295delinsACA GRCh38
NC_000009.11:g.136149709_136149711delinsACA , CM000671.1:g.136149709_136149711delinsACA GRCh37
NC_000009.10:g.135139530_135139532delinsACA NCBI36
NG_006669.2:g.5920_5922delinsTGT

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+867_58+869delinsTGT
ENST00000647353.1:n.53+867_53+869delinsTGT
ENST00000651471.1:n.63+1667_63+1669delinsTGT
ENST00000679909.1:c.28+867_28+869delinsTGT ENSP00000506089.1:n.28+867_28+869delinsTG...
ENST00000453660.3:n.40+867_40+869delinsTGT
ENST00000538324.2:c.28+867_28+869delinsTGT ENSP00000483018.1:n.28+867_28+869delinsTG...
ENST00000611156.4:c.28+867_28+869delinsTGT ENSP00000483265.1:n.28+867_28+869delinsTG...
NM_020469.2:c.28+867_28+869delinsTGT NP_065202.2:n.28+867_28+869delinsTGT
NM_020469.3:c.28+867_28+869delinsTGT NP_065202.2:n.28+867_28+869delinsTGT