Canonical Allele Identifier: CA2579497348
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256093_133256104dup , CM000671.2:g.133256093_133256104dup GRCh38
NC_000009.11:g.136131480_136131491dup , CM000671.1:g.136131480_136131491dup GRCh37
NC_000009.10:g.135121301_135121312dup NCBI36
NG_006669.1:g.21565_21576dup
NG_006669.2:g.24113_24124dup

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.657_668dup
ENST00000647353.1:n.54-4951_54-4940dup
ENST00000679909.1:c.28+19059_28+19070dup ENSP00000506089.1:n.28+19059_28+19070dup
ENST00000453660.3:n.639_650dup
ENST00000538324.2:c.625_636dup ENSP00000483018.1:p.Asp212_Met213insValAs...
ENST00000611156.4:c.625_636dup ENSP00000483265.1:p.Asp212_Met213insValAs...
NM_020469.2:c.628_639dup NP_065202.2:p.Asp213_Met214insValAspValAs...
NM_020469.3:c.628_639dup NP_065202.2:p.Asp213_Met214insValAspValAs...