Canonical Allele Identifier: CA860751017

Gene: ABO

Linked Data

• dbSNP Id: rs1242266618
• MyVariant Identifiers: chr9:g.136130774_136130777del (hg19) ; chr9:g.133255387_133255390del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255390_133255393del , CM000671.2:g.133255390_133255393del	GRCh38
NC_000009.11:g.136130777_136130780del , CM000671.1:g.136130777_136130780del	GRCh37
NC_000009.10:g.135120598_135120601del	NCBI36
NG_006669.1:g.22278_22281del
NG_006669.2:g.24826_24829del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1370_1373del
ENST00000647353.1:n.54-4238_54-4235del
ENST00000679909.1:c.28+19772_28+19775del	ENSP00000506089.1:n.28+19772_28+19775del
ENST00000453660.3:n.1352_1355del
ENST00000611156.4:c.*276_*279del	ENSP00000483265.1:n.*276_*279del
NM_020469.2:c.*276_*279del	NP_065202.2:n.*276_*279del
NM_020469.3:c.*276_*279del	NP_065202.2:n.*276_*279del