Canonical Allele Identifier: CA1882578594
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255386_133255390delinsGTCTT , CM000671.2:g.133255386_133255390delinsGTCTT GRCh38
NC_000009.11:g.136130773_136130777delinsGTCTT , CM000671.1:g.136130773_136130777delinsGTCTT GRCh37
NC_000009.10:g.135120594_135120598delinsGTCTT NCBI36
NG_006669.1:g.22278_22282delinsAAGAC
NG_006669.2:g.24826_24830delinsAAGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1370_1374delinsAAGAC
ENST00000647353.1:n.54-4238_54-4234delinsAAGAC
ENST00000679909.1:c.28+19772_28+19776delinsAAGAC ENSP00000506089.1:n.28+19772_28+19776delinsAAGAC
ENST00000453660.3:n.1352_1356delinsAAGAC
ENST00000611156.4:c.*276_*280delinsAAGAC ENSP00000483265.1:n.*276_*280delinsAAGAC
NM_020469.2:c.*276_*280delinsAAGAC NP_065202.2:n.*276_*280delinsAAGAC
NM_020469.3:c.*276_*280delinsAAGAC NP_065202.2:n.*276_*280delinsAAGAC