Canonical Allele Identifier: CA1882590599

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133274209_133274210delinsAG , CM000671.2:g.133274209_133274210delinsAG	GRCh38
NC_000009.11:g.136149625_136149626delinsAG , CM000671.1:g.136149625_136149626delinsAG	GRCh37
NC_000009.10:g.135139446_135139447delinsAG	NCBI36
NG_006669.1:g.3425_3426delinsCT
NG_006669.2:g.6005_6006delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.58+952_58+953delinsCT
ENST00000647353.1:n.53+952_53+953delinsCT
ENST00000651471.1:n.63+1752_63+1753delinsCT
ENST00000679909.1:c.28+952_28+953delinsCT	ENSP00000506089.1:n.28+952_28+953delinsCT...
ENST00000453660.3:n.40+952_40+953delinsCT
ENST00000538324.2:c.28+952_28+953delinsCT	ENSP00000483018.1:n.28+952_28+953delinsCT...
ENST00000611156.4:c.28+952_28+953delinsCT	ENSP00000483265.1:n.28+952_28+953delinsCT...
NM_020469.2:c.28+952_28+953delinsCT	NP_065202.2:n.28+952_28+953delinsCT
NM_020469.3:c.28+952_28+953delinsCT	NP_065202.2:n.28+952_28+953delinsCT