Canonical Allele Identifier: CA918570289

Gene: ABO

Linked Data

• dbSNP Id: rs1564303328

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255437_133255438delinsGC , CM000671.2:g.133255437_133255438delinsGC	GRCh38
NC_000009.11:g.136130824_136130825delinsGC , CM000671.1:g.136130824_136130825delinsGC	GRCh37
NC_000009.10:g.135120645_135120646delinsGC	NCBI36
NG_006669.1:g.22230_22231delinsGC
NG_006669.2:g.24778_24779delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1322_1323delinsGC
ENST00000647353.1:n.54-4286_54-4285delinsGC
ENST00000679909.1:c.28+19724_28+19725delinsGC	ENSP00000506089.1:n.28+19724_28+19725delinsGC
ENST00000453660.3:n.1304_1305delinsGC
ENST00000611156.4:c.*228_*229delinsGC	ENSP00000483265.1:n.*228_*229delinsGC
NM_020469.2:c.*228_*229delinsGC	NP_065202.2:n.*228_*229delinsGC
NM_020469.3:c.*228_*229delinsGC	NP_065202.2:n.*228_*229delinsGC