Canonical Allele Identifier: CA1882584439
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260300_133260301delinsCT , CM000671.2:g.133260300_133260301delinsCT GRCh38
NC_000009.11:g.136135703_136135704delinsCT , CM000671.1:g.136135703_136135704delinsCT GRCh37
NC_000009.10:g.135125524_135125525delinsCT NCBI36
NG_006669.1:g.17349_17350delinsAG
NG_006669.2:g.19914_19915delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.186-435_186-434delinsAG
ENST00000647353.1:n.54-9149_54-9148delinsAG
ENST00000651471.1:n.191-435_191-434delinsAG
ENST00000679909.1:c.28+14861_28+14862delinsAG ENSP00000506089.1:n.28+14861_28+14862deli...
ENST00000453660.3:n.168-435_168-434delinsAG
ENST00000538324.2:c.156-435_156-434delinsAG ENSP00000483018.1:n.156-435_156-434delins...
ENST00000611156.4:c.156-435_156-434delinsAG ENSP00000483265.1:n.156-435_156-434delins...
NM_020469.2:c.156-435_156-434delinsAG NP_065202.2:n.156-435_156-434delinsAG
NM_020469.3:c.156-435_156-434delinsAG NP_065202.2:n.156-435_156-434delinsAG