Canonical Allele Identifier: CA1882582610
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257674_133257675delinsAG , CM000671.2:g.133257674_133257675delinsAG GRCh38
NC_000009.11:g.136133061_136133062delinsAG , CM000671.1:g.136133061_136133062delinsAG GRCh37
NC_000009.10:g.135122882_135122883delinsAG NCBI36
NG_006669.1:g.19992_19993delinsCT
NG_006669.2:g.22540_22541delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-133_270-132delinsCT
ENST00000647353.1:n.54-6523_54-6522delinsCT
ENST00000651471.1:n.329+367_329+368delinsCT
ENST00000679909.1:c.28+17487_28+17488delinsCT ENSP00000506089.1:n.28+17487_28+17488delinsCT
ENST00000453660.3:n.252-133_252-132delinsCT
ENST00000538324.2:c.240-133_240-132delinsCT ENSP00000483018.1:n.240-133_240-132delinsCT
ENST00000611156.4:c.240-133_240-132delinsCT ENSP00000483265.1:n.240-133_240-132delinsCT
NM_020469.2:c.240-133_240-132delinsCT NP_065202.2:n.240-133_240-132delinsCT
NM_020469.3:c.240-133_240-132delinsCT NP_065202.2:n.240-133_240-132delinsCT