Canonical Allele Identifier: CA860752481

Gene: ABO

Linked Data

• dbSNP Id: rs1487690291
• MyVariant Identifiers: chr9:g.136131386_136131388del (hg19) ; chr9:g.133255999_133256001del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256000_133256002del , CM000671.2:g.133256000_133256002del	GRCh38
NC_000009.11:g.136131387_136131389del , CM000671.1:g.136131387_136131389del	GRCh37
NC_000009.10:g.135121208_135121210del	NCBI36
NG_006669.1:g.21667_21669del
NG_006669.2:g.24215_24217del

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.759_761del
ENST00000647353.1:n.54-4849_54-4847del
ENST00000679909.1:c.28+19161_28+19163del	ENSP00000506089.1:n.28+19161_28+19163del
ENST00000453660.3:n.741_743del
ENST00000538324.2:c.727_729del	ENSP00000483018.1:p.Phe243del
ENST00000611156.4:c.727_729del	ENSP00000483265.1:p.Phe243del
NM_020469.2:c.730_732del	NP_065202.2:p.Phe244del
NM_020469.3:c.730_732del	NP_065202.2:p.Phe244del