Canonical Allele Identifier: CA1129724765
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274124_133274125insAAT , CM000671.2:g.133274124_133274125insAAT GRCh38
NC_000009.11:g.136149540_136149541insAAT , CM000671.1:g.136149540_136149541insAAT GRCh37
NC_000009.10:g.135139361_135139362insAAT NCBI36
NG_006669.1:g.3511_3512insTTA
NG_006669.2:g.6091_6092insTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+1038_58+1039insTTA
ENST00000647353.1:n.53+1038_53+1039insTTA
ENST00000651471.1:n.63+1838_63+1839insTTA
ENST00000679909.1:c.28+1038_28+1039insTTA ENSP00000506089.1:n.28+1038_28+1039insTTA...
ENST00000453660.3:n.40+1038_40+1039insTTA
ENST00000538324.2:c.28+1038_28+1039insTTA ENSP00000483018.1:n.28+1038_28+1039insTTA...
ENST00000611156.4:c.28+1038_28+1039insTTA ENSP00000483265.1:n.28+1038_28+1039insTTA...
NM_020469.2:c.28+1038_28+1039insTTA NP_065202.2:n.28+1038_28+1039insTTA
NM_020469.3:c.28+1038_28+1039insTTA NP_065202.2:n.28+1038_28+1039insTTA