Canonical Allele Identifier: CA1882578698
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255437_133255438delinsTG , CM000671.2:g.133255437_133255438delinsTG GRCh38
NC_000009.11:g.136130824_136130825delinsTG , CM000671.1:g.136130824_136130825delinsTG GRCh37
NC_000009.10:g.135120645_135120646delinsTG NCBI36
NG_006669.1:g.22230_22231delinsCA
NG_006669.2:g.24778_24779delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1322_1323delinsCA
ENST00000647353.1:n.54-4286_54-4285delinsCA
ENST00000679909.1:c.28+19724_28+19725delinsCA ENSP00000506089.1:n.28+19724_28+19725delinsCA
ENST00000453660.3:n.1304_1305delinsCA
ENST00000611156.4:c.*228_*229delinsCA ENSP00000483265.1:n.*228_*229delinsCA
NM_020469.2:c.*228_*229delinsCA NP_065202.2:n.*228_*229delinsCA
NM_020469.3:c.*228_*229delinsCA NP_065202.2:n.*228_*229delinsCA