Canonical Allele Identifier: CA1882584379
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260131_133260139delinsACGTCGAAG , CM000671.2:g.133260131_133260139delinsACGTCGAAG GRCh38
NC_000009.11:g.136135535_136135543delinsACGTCGAAG , CM000671.1:g.136135535_136135543delinsACGTCGAAG GRCh37
NC_000009.10:g.135125356_135125364delinsACGTCGAAG NCBI36
NG_006669.1:g.17511_17519delinsCTTCGACGT
NG_006669.2:g.20076_20084delinsCTTCGACGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.186-273_186-265delinsCTTCGACGT
ENST00000647353.1:n.54-8987_54-8979delinsCTTCGACGT
ENST00000651471.1:n.191-273_191-265delinsCTTCGACGT
ENST00000679909.1:c.28+15023_28+15031delinsCTTCGACGT ENSP00000506089.1:n.28+15023_28+15031delinsCTTCGACGT
ENST00000453660.3:n.168-273_168-265delinsCTTCGACGT
ENST00000538324.2:c.156-273_156-265delinsCTTCGACGT ENSP00000483018.1:n.156-273_156-265delinsCTTCGACGT
ENST00000611156.4:c.156-273_156-265delinsCTTCGACGT ENSP00000483265.1:n.156-273_156-265delinsCTTCGACGT
NM_020469.2:c.156-273_156-265delinsCTTCGACGT NP_065202.2:n.156-273_156-265delinsCTTCGACGT
NM_020469.3:c.156-273_156-265delinsCTTCGACGT NP_065202.2:n.156-273_156-265delinsCTTCGACGT