Canonical Allele Identifier: CA1882578536
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255369_133255373delinsTGTGA , CM000671.2:g.133255369_133255373delinsTGTGA GRCh38
NC_000009.11:g.136130756_136130760delinsTGTGA , CM000671.1:g.136130756_136130760delinsTGTGA GRCh37
NC_000009.10:g.135120577_135120581delinsTGTGA NCBI36
NG_006669.1:g.22295_22299delinsTCACA
NG_006669.2:g.24843_24847delinsTCACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1387_1391delinsTCACA
ENST00000647353.1:n.54-4221_54-4217delinsTCACA
ENST00000679909.1:c.28+19789_28+19793delinsTCACA ENSP00000506089.1:n.28+19789_28+19793delinsTCACA
ENST00000453660.3:n.1369_1373delinsTCACA
ENST00000611156.4:c.*293_*297delinsTCACA ENSP00000483265.1:n.*293_*297delinsTCACA
NM_020469.2:c.*293_*297delinsTCACA NP_065202.2:n.*293_*297delinsTCACA
NM_020469.3:c.*293_*297delinsTCACA NP_065202.2:n.*293_*297delinsTCACA