Canonical Allele Identifier: CA1882580023
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255964_133255973delinsATGTAGGCCT , CM000671.2:g.133255964_133255973delinsATGTAGGCCT GRCh38
NC_000009.11:g.136131351_136131360delinsATGTAGGCCT , CM000671.1:g.136131351_136131360delinsATGTAGGCCT GRCh37
NC_000009.10:g.135121172_135121181delinsATGTAGGCCT NCBI36
NG_006669.1:g.21695_21704delinsAGGCCTACAT
NG_006669.2:g.24243_24252delinsAGGCCTACAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.787_796delinsAGGCCTACAT
ENST00000647353.1:n.54-4821_54-4812delinsAGGCCTACAT
ENST00000679909.1:c.28+19189_28+19198delinsAGGCCTACAT ENSP00000506089.1:n.28+19189_28+19198delinsAGGCCTACAT
ENST00000453660.3:n.769_778delinsAGGCCTACAT
ENST00000538324.2:c.755_764delinsAGGCCTACAT ENSP00000483018.1:p.Gln252=
ENST00000611156.4:c.755_764delinsAGGCCTACAT ENSP00000483265.1:p.Gln252=
NM_020469.2:c.758_767delinsAGGCCTACAT NP_065202.2:p.Gln253=
NM_020469.3:c.758_767delinsAGGCCTACAT NP_065202.2:p.Gln253=