Canonical Allele Identifier: CA1882578675
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255418_133255420delinsGTC , CM000671.2:g.133255418_133255420delinsGTC GRCh38
NC_000009.11:g.136130805_136130807delinsGTC , CM000671.1:g.136130805_136130807delinsGTC GRCh37
NC_000009.10:g.135120626_135120628delinsGTC NCBI36
NG_006669.1:g.22248_22250delinsGAC
NG_006669.2:g.24796_24798delinsGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1340_1342delinsGAC
ENST00000647353.1:n.54-4268_54-4266delinsGAC
ENST00000679909.1:c.28+19742_28+19744delinsGAC ENSP00000506089.1:n.28+19742_28+19744delinsGAC
ENST00000453660.3:n.1322_1324delinsGAC
ENST00000611156.4:c.*246_*248delinsGAC ENSP00000483265.1:n.*246_*248delinsGAC
NM_020469.2:c.*246_*248delinsGAC NP_065202.2:n.*246_*248delinsGAC
NM_020469.3:c.*246_*248delinsGAC NP_065202.2:n.*246_*248delinsGAC