Canonical Allele Identifier: CA1882578423
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255332_133255334delinsATG , CM000671.2:g.133255332_133255334delinsATG GRCh38
NC_000009.11:g.136130719_136130721delinsATG , CM000671.1:g.136130719_136130721delinsATG GRCh37
NC_000009.10:g.135120540_135120542delinsATG NCBI36
NG_006669.1:g.22334_22336delinsCAT
NG_006669.2:g.24882_24884delinsCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1426_1428delinsCAT
ENST00000647353.1:n.54-4182_54-4180delinsCAT
ENST00000679909.1:c.28+19828_28+19830delinsCAT ENSP00000506089.1:n.28+19828_28+19830delinsCAT
ENST00000453660.3:n.1408_1410delinsCAT
ENST00000611156.4:c.*332_*334delinsCAT ENSP00000483265.1:n.*332_*334delinsCAT
NM_020469.2:c.*332_*334delinsCAT NP_065202.2:n.*332_*334delinsCAT
NM_020469.3:c.*332_*334delinsCAT NP_065202.2:n.*332_*334delinsCAT