Canonical Allele Identifier: CA1882585008
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133261595_133261598delinsCTCA , CM000671.2:g.133261595_133261598delinsCTCA GRCh38
NC_000009.11:g.136136998_136137001delinsCTCA , CM000671.1:g.136136998_136137001delinsCTCA GRCh37
NC_000009.10:g.135126819_135126822delinsCTCA NCBI36
NG_006669.1:g.16052_16055delinsTGAG
NG_006669.2:g.18617_18620delinsTGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.129-224_129-221delinsTGAG
ENST00000647353.1:n.54-10446_54-10443delinsTGAG
ENST00000651471.1:n.134-224_134-221delinsTGAG
ENST00000679909.1:c.28+13564_28+13567delinsTGAG ENSP00000506089.1:n.28+13564_28+13567delinsTGAG
ENST00000453660.3:n.111-224_111-221delinsTGAG
ENST00000538324.2:c.99-224_99-221delinsTGAG ENSP00000483018.1:n.99-224_99-221delinsTGAG
ENST00000611156.4:c.99-224_99-221delinsTGAG ENSP00000483265.1:n.99-224_99-221delinsTGAG
NM_020469.2:c.99-224_99-221delinsTGAG NP_065202.2:n.99-224_99-221delinsTGAG
NM_020469.3:c.99-224_99-221delinsTGAG NP_065202.2:n.99-224_99-221delinsTGAG