Canonical Allele Identifier: CA5305782
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs782433608

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256099_133256104dup , CM000671.2:g.133256099_133256104dup GRCh38
NC_000009.11:g.136131486_136131491dup , CM000671.1:g.136131486_136131491dup GRCh37
NC_000009.10:g.135121307_135121312dup NCBI36
NG_006669.1:g.21571_21576dup
NG_006669.2:g.24119_24124dup

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.663_668dup
ENST00000647353.1:n.54-4945_54-4940dup
ENST00000679909.1:c.28+19065_28+19070dup ENSP00000506089.1:n.28+19065_28+19070dup
ENST00000453660.3:n.645_650dup
ENST00000538324.2:c.631_636dup ENSP00000483018.1:p.Asp212_Met213insValAs...
ENST00000611156.4:c.631_636dup ENSP00000483265.1:p.Asp212_Met213insValAs...
NM_020469.2:c.634_639dup NP_065202.2:p.Asp213_Met214insValAsp
NM_020469.3:c.634_639dup NP_065202.2:p.Asp213_Met214insValAsp