Canonical Allele Identifier: CA2786163478

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133261625_133261632del , CM000671.2:g.133261625_133261632del	GRCh38
NC_000009.11:g.136137028_136137035del , CM000671.1:g.136137028_136137035del	GRCh37
NC_000009.10:g.135126849_135126856del	NCBI36
NG_006669.1:g.16022_16029del
NG_006669.2:g.18587_18594del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.129-254_129-247del
ENST00000647353.1:n.54-10476_54-10469del
ENST00000651471.1:n.134-254_134-247del
ENST00000679909.1:c.28+13534_28+13541del	ENSP00000506089.1:n.28+13534_28+13541del
ENST00000453660.3:n.111-254_111-247del
ENST00000538324.2:c.99-254_99-247del	ENSP00000483018.1:n.99-254_99-247del
ENST00000611156.4:c.99-254_99-247del	ENSP00000483265.1:n.99-254_99-247del
NM_020469.2:c.99-254_99-247del	NP_065202.2:n.99-254_99-247del
NM_020469.3:c.99-254_99-247del	NP_065202.2:n.99-254_99-247del