Canonical Allele Identifier: CA2786162875
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255359_133255361del , CM000671.2:g.133255359_133255361del GRCh38
NC_000009.11:g.136130746_136130748del , CM000671.1:g.136130746_136130748del GRCh37
NC_000009.10:g.135120567_135120569del NCBI36
NG_006669.1:g.22309_22311del
NG_006669.2:g.24857_24859del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1401_1403del
ENST00000647353.1:n.54-4207_54-4205del
ENST00000679909.1:c.28+19803_28+19805del ENSP00000506089.1:n.28+19803_28+19805del
ENST00000453660.3:n.1383_1385del
ENST00000611156.4:c.*307_*309del ENSP00000483265.1:n.*307_*309del
NM_020469.2:c.*307_*309del NP_065202.2:n.*307_*309del
NM_020469.3:c.*307_*309del NP_065202.2:n.*307_*309del