Canonical Allele Identifier: CA1882580373
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256111_133256112delinsAG , CM000671.2:g.133256111_133256112delinsAG GRCh38
NC_000009.11:g.136131498_136131499delinsAG , CM000671.1:g.136131498_136131499delinsAG GRCh37
NC_000009.10:g.135121319_135121320delinsAG NCBI36
NG_006669.1:g.21556_21557delinsCT
NG_006669.2:g.24104_24105delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.648_649delinsCT
ENST00000647353.1:n.54-4960_54-4959delinsCT
ENST00000651471.1:n.574_575delinsCT
ENST00000679909.1:c.28+19050_28+19051delinsCT ENSP00000506089.1:n.28+19050_28+19051delinsCT
ENST00000453660.3:n.630_631delinsCT
ENST00000538324.2:c.616_617delinsCT ENSP00000483018.1:p.Leu206=
ENST00000611156.4:c.616_617delinsCT ENSP00000483265.1:p.Leu206=
NM_020469.2:c.619_620delinsCT NP_065202.2:p.Leu207=
NM_020469.3:c.619_620delinsCT NP_065202.2:p.Leu207=