Canonical Allele Identifier: CA1882583191

Gene: ABO

Linked Data

• dbSNP Id: rs1834637080
• gnomAD v4: 9-133258155-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258156del , CM000671.2:g.133258156del	GRCh38
NC_000009.11:g.136133546del , CM000671.1:g.136133546del	GRCh37
NC_000009.10:g.135123367del	NCBI36
NG_006669.1:g.19508del
NG_006669.2:g.22059del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.234-24del
ENST00000647353.1:n.54-7004del
ENST00000651471.1:n.239-24del
ENST00000679909.1:c.28+17006del	ENSP00000506089.1:n.28+17006del
ENST00000453660.3:n.216-24del
ENST00000538324.2:c.204-24del	ENSP00000483018.1:n.204-24del
ENST00000611156.4:c.204-24del	ENSP00000483265.1:n.204-24del
NM_020469.2:c.204-24del	NP_065202.2:n.204-24del
NM_020469.3:c.204-24del	NP_065202.2:n.204-24del