Canonical Allele Identifier: CA2579497345
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255643_133255644insCG , CM000671.2:g.133255643_133255644insCG GRCh38
NC_000009.11:g.136131030_136131031insCG , CM000671.1:g.136131030_136131031insCG GRCh37
NC_000009.10:g.135120851_135120852insCG NCBI36
NG_006669.1:g.22024_22025insCG
NG_006669.2:g.24572_24573insCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1116_1117insCG
ENST00000647353.1:n.54-4492_54-4491insCG
ENST00000679909.1:c.28+19518_28+19519insCG ENSP00000506089.1:n.28+19518_28+19519insCG
ENST00000453660.3:n.1098_1099insCG
ENST00000538324.2:c.1080_1081insCG ENSP00000483018.1:p.Gly361ArgfsTer?
ENST00000611156.4:c.*22_*23insCG ENSP00000483265.1:n.*22_*23insCG
NM_020469.2:c.*22_*23insCG NP_065202.2:n.*22_*23insCG
NM_020469.3:c.*22_*23insCG NP_065202.2:n.*22_*23insCG