Canonical Allele Identifier: CA1882578564
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255380_133255390delinsGTCTGTGTCTT , CM000671.2:g.133255380_133255390delinsGTCTGTGTCTT GRCh38
NC_000009.11:g.136130767_136130777delinsGTCTGTGTCTT , CM000671.1:g.136130767_136130777delinsGTCTGTGTCTT GRCh37
NC_000009.10:g.135120588_135120598delinsGTCTGTGTCTT NCBI36
NG_006669.1:g.22278_22288delinsAAGACACAGAC
NG_006669.2:g.24826_24836delinsAAGACACAGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1370_1380delinsAAGACACAGAC
ENST00000647353.1:n.54-4238_54-4228delinsAAGACACAGAC
ENST00000679909.1:c.28+19772_28+19782delinsAAGACACAGAC ENSP00000506089.1:n.28+19772_28+19782delinsAAGACACAGAC
ENST00000453660.3:n.1352_1362delinsAAGACACAGAC
ENST00000611156.4:c.*276_*286delinsAAGACACAGAC ENSP00000483265.1:n.*276_*286delinsAAGACACAGAC
NM_020469.2:c.*276_*286delinsAAGACACAGAC NP_065202.2:n.*276_*286delinsAAGACACAGAC
NM_020469.3:c.*276_*286delinsAAGACACAGAC NP_065202.2:n.*276_*286delinsAAGACACAGAC