Canonical Allele Identifier: CA1882584413
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260221_133260223delinsCTG , CM000671.2:g.133260221_133260223delinsCTG GRCh38
NC_000009.11:g.136135625_136135627delinsCTG , CM000671.1:g.136135625_136135627delinsCTG GRCh37
NC_000009.10:g.135125446_135125448delinsCTG NCBI36
NG_006669.1:g.17427_17429delinsCAG
NG_006669.2:g.19992_19994delinsCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.186-357_186-355delinsCAG
ENST00000647353.1:n.54-9071_54-9069delinsCAG
ENST00000651471.1:n.191-357_191-355delinsCAG
ENST00000679909.1:c.28+14939_28+14941delinsCAG ENSP00000506089.1:n.28+14939_28+14941delinsCAG
ENST00000453660.3:n.168-357_168-355delinsCAG
ENST00000538324.2:c.156-357_156-355delinsCAG ENSP00000483018.1:n.156-357_156-355delinsCAG
ENST00000611156.4:c.156-357_156-355delinsCAG ENSP00000483265.1:n.156-357_156-355delinsCAG
NM_020469.2:c.156-357_156-355delinsCAG NP_065202.2:n.156-357_156-355delinsCAG
NM_020469.3:c.156-357_156-355delinsCAG NP_065202.2:n.156-357_156-355delinsCAG