Canonical Allele Identifier: CA1882585019

Gene: ABO

Linked Data

• dbSNP Id: rs1834712157

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133261608_133261609insGG , CM000671.2:g.133261608_133261609insGG	GRCh38
NC_000009.11:g.136137011_136137012insGG , CM000671.1:g.136137011_136137012insGG	GRCh37
NC_000009.10:g.135126832_135126833insGG	NCBI36
NG_006669.1:g.16041_16042insCC
NG_006669.2:g.18606_18607insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.129-235_129-234insCC
ENST00000647353.1:n.54-10457_54-10456insCC
ENST00000651471.1:n.134-235_134-234insCC
ENST00000679909.1:c.28+13553_28+13554insCC	ENSP00000506089.1:n.28+13553_28+13554insCC
ENST00000453660.3:n.111-235_111-234insCC
ENST00000538324.2:c.99-235_99-234insCC	ENSP00000483018.1:n.99-235_99-234insCC
ENST00000611156.4:c.99-235_99-234insCC	ENSP00000483265.1:n.99-235_99-234insCC
NM_020469.2:c.99-235_99-234insCC	NP_065202.2:n.99-235_99-234insCC
NM_020469.3:c.99-235_99-234insCC	NP_065202.2:n.99-235_99-234insCC