Canonical Allele Identifier: CA200764872

Gene: ABO

Linked Data

• dbSNP Id: rs766488977
• MyVariant Identifiers: chr9:g.136130762_136130781del (hg19) ; chr9:g.133255375_133255394del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255376_133255395del , CM000671.2:g.133255376_133255395del	GRCh38
NC_000009.11:g.136130763_136130782del , CM000671.1:g.136130763_136130782del	GRCh37
NC_000009.10:g.135120584_135120603del	NCBI36
NG_006669.1:g.22274_22293del
NG_006669.2:g.24822_24841del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1366_1385del
ENST00000647353.1:n.54-4242_54-4223del
ENST00000679909.1:c.28+19768_28+19787del	ENSP00000506089.1:n.28+19768_28+19787del
ENST00000453660.3:n.1348_1367del
ENST00000611156.4:c.*272_*291del	ENSP00000483265.1:n.*272_*291del
NM_020469.2:c.*272_*291del	NP_065202.2:n.*272_*291del
NM_020469.3:c.*272_*291del	NP_065202.2:n.*272_*291del