Canonical Allele Identifier: CA2720571365

Gene: ABO

Linked Data

• dbSNP Id: rs2118989815

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133274035_133274038del , CM000671.2:g.133274035_133274038del	GRCh38
NC_000009.11:g.136149451_136149454del , CM000671.1:g.136149451_136149454del	GRCh37
NC_000009.10:g.135139272_135139275del	NCBI36
NG_006669.1:g.3600_3603del
NG_006669.2:g.6180_6183del

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.58+1127_58+1130del
ENST00000647353.1:n.53+1127_53+1130del
ENST00000651471.1:n.63+1927_63+1930del
ENST00000679909.1:c.28+1127_28+1130del	ENSP00000506089.1:n.28+1127_28+1130del
ENST00000453660.3:n.40+1127_40+1130del
ENST00000538324.2:c.28+1127_28+1130del	ENSP00000483018.1:n.28+1127_28+1130del
ENST00000611156.4:c.28+1127_28+1130del	ENSP00000483265.1:n.28+1127_28+1130del
NM_020469.2:c.28+1127_28+1130del	NP_065202.2:n.28+1127_28+1130del
NM_020469.3:c.28+1127_28+1130del	NP_065202.2:n.28+1127_28+1130del