Canonical Allele Identifier: CA2507416379

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133274133_133274134insGG , CM000671.2:g.133274133_133274134insGG	GRCh38
NC_000009.11:g.136149549_136149550insGG , CM000671.1:g.136149549_136149550insGG	GRCh37
NC_000009.10:g.135139370_135139371insGG	NCBI36
NG_006669.1:g.3501_3502insCC
NG_006669.2:g.6081_6082insCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.58+1028_58+1029insCC
ENST00000647353.1:n.53+1028_53+1029insCC
ENST00000651471.1:n.63+1828_63+1829insCC
ENST00000679909.1:c.28+1028_28+1029insCC	ENSP00000506089.1:n.28+1028_28+1029insCC
ENST00000453660.3:n.40+1028_40+1029insCC
ENST00000538324.2:c.28+1028_28+1029insCC	ENSP00000483018.1:n.28+1028_28+1029insCC
ENST00000611156.4:c.28+1028_28+1029insCC	ENSP00000483265.1:n.28+1028_28+1029insCC
NM_020469.2:c.28+1028_28+1029insCC	NP_065202.2:n.28+1028_28+1029insCC
NM_020469.3:c.28+1028_28+1029insCC	NP_065202.2:n.28+1028_28+1029insCC