Canonical Allele Identifier: CA1882579187
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255657_133255663delinsGGCAGCC , CM000671.2:g.133255657_133255663delinsGGCAGCC GRCh38
NC_000009.11:g.136131044_136131050delinsGGCAGCC , CM000671.1:g.136131044_136131050delinsGGCAGCC GRCh37
NC_000009.10:g.135120865_135120871delinsGGCAGCC NCBI36
NG_006669.1:g.22005_22011delinsGGCTGCC
NG_006669.2:g.24553_24559delinsGGCTGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1097_1103delinsGGCTGCC
ENST00000647353.1:n.54-4511_54-4505delinsGGCTGCC
ENST00000679909.1:c.28+19499_28+19505delinsGGCTGCC ENSP00000506089.1:n.28+19499_28+19505delinsGGCTGCC
ENST00000453660.3:n.1079_1085delinsGGCTGCC
ENST00000538324.2:c.1061_1067delinsGGCTGCC ENSP00000483018.1:p.Arg354=
ENST00000611156.4:c.*3_*9delinsGGCTGCC ENSP00000483265.1:n.*3_*9delinsGGCTGCC
NM_020469.2:c.*3_*9delinsGGCTGCC NP_065202.2:n.*3_*9delinsGGCTGCC
NM_020469.3:c.*3_*9delinsGGCTGCC NP_065202.2:n.*3_*9delinsGGCTGCC