Canonical Allele Identifier: CA1882578445
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255339_133255341delinsGGT , CM000671.2:g.133255339_133255341delinsGGT GRCh38
NC_000009.11:g.136130726_136130728delinsGGT , CM000671.1:g.136130726_136130728delinsGGT GRCh37
NC_000009.10:g.135120547_135120549delinsGGT NCBI36
NG_006669.1:g.22327_22329delinsACC
NG_006669.2:g.24875_24877delinsACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1419_1421delinsACC
ENST00000647353.1:n.54-4189_54-4187delinsACC
ENST00000679909.1:c.28+19821_28+19823delinsACC ENSP00000506089.1:n.28+19821_28+19823delinsACC
ENST00000453660.3:n.1401_1403delinsACC
ENST00000611156.4:c.*325_*327delinsACC ENSP00000483265.1:n.*325_*327delinsACC
NM_020469.2:c.*325_*327delinsACC NP_065202.2:n.*325_*327delinsACC
NM_020469.3:c.*325_*327delinsACC NP_065202.2:n.*325_*327delinsACC