Canonical Allele Identifier: CA2786162846
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255288_133255289del , CM000671.2:g.133255288_133255289del GRCh38
NC_000009.11:g.136130675_136130676del , CM000671.1:g.136130675_136130676del GRCh37
NC_000009.10:g.135120496_135120497del NCBI36
NG_006669.1:g.22383_22384del
NG_006669.2:g.24931_24932del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1475_1476del
ENST00000647353.1:n.54-4133_54-4132del
ENST00000679909.1:c.28+19877_28+19878del ENSP00000506089.1:n.28+19877_28+19878del
ENST00000453660.3:n.1457_1458del
ENST00000611156.4:c.*381_*382del ENSP00000483265.1:n.*381_*382del
NM_020469.2:c.*381_*382del NP_065202.2:n.*381_*382del
NM_020469.3:c.*381_*382del NP_065202.2:n.*381_*382del