Canonical Allele Identifier: CA1882578580
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255382_133255384delinsCTG , CM000671.2:g.133255382_133255384delinsCTG GRCh38
NC_000009.11:g.136130769_136130771delinsCTG , CM000671.1:g.136130769_136130771delinsCTG GRCh37
NC_000009.10:g.135120590_135120592delinsCTG NCBI36
NG_006669.1:g.22284_22286delinsCAG
NG_006669.2:g.24832_24834delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1376_1378delinsCAG
ENST00000647353.1:n.54-4232_54-4230delinsCAG
ENST00000679909.1:c.28+19778_28+19780delinsCAG ENSP00000506089.1:n.28+19778_28+19780delinsCAG
ENST00000453660.3:n.1358_1360delinsCAG
ENST00000611156.4:c.*282_*284delinsCAG ENSP00000483265.1:n.*282_*284delinsCAG
NM_020469.2:c.*282_*284delinsCAG NP_065202.2:n.*282_*284delinsCAG
NM_020469.3:c.*282_*284delinsCAG NP_065202.2:n.*282_*284delinsCAG