Canonical Allele Identifier: CA1882585220
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133262062_133262064delinsCAA , CM000671.2:g.133262062_133262064delinsCAA GRCh38
NC_000009.11:g.136137465_136137467delinsCAA , CM000671.1:g.136137465_136137467delinsCAA GRCh37
NC_000009.10:g.135127286_135127288delinsCAA NCBI36
NG_006669.1:g.15585_15587delinsTTG
NG_006669.2:g.18151_18153delinsTTG

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.128+35_128+37delinsTTG
ENST00000647353.1:n.54-10912_54-10910delinsTTG
ENST00000651471.1:n.133+35_133+37delinsTTG
ENST00000679909.1:c.28+13098_28+13100delinsTTG ENSP00000506089.1:n.28+13098_28+13100deli...
ENST00000453660.3:n.110+35_110+37delinsTTG
ENST00000538324.2:c.98+35_98+37delinsTTG ENSP00000483018.1:n.98+35_98+37delinsTTG
ENST00000611156.4:c.98+35_98+37delinsTTG ENSP00000483265.1:n.98+35_98+37delinsTTG
NM_020469.2:c.98+35_98+37delinsTTG NP_065202.2:n.98+35_98+37delinsTTG
NM_020469.3:c.98+35_98+37delinsTTG NP_065202.2:n.98+35_98+37delinsTTG