Canonical Allele Identifier: CA1882578518

Gene: ABO

Linked Data

• dbSNP Id: rs1834546178
• gnomAD v4: 9-133255361-GGTGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255369_133255372del , CM000671.2:g.133255369_133255372del	GRCh38
NC_000009.11:g.136130756_136130759del , CM000671.1:g.136130756_136130759del	GRCh37
NC_000009.10:g.135120577_135120580del	NCBI36
NG_006669.1:g.22303_22306del
NG_006669.2:g.24851_24854del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1395_1398del
ENST00000647353.1:n.54-4213_54-4210del
ENST00000679909.1:c.28+19797_28+19800del	ENSP00000506089.1:n.28+19797_28+19800del
ENST00000453660.3:n.1377_1380del
ENST00000611156.4:c.*301_*304del	ENSP00000483265.1:n.*301_*304del
NM_020469.2:c.*301_*304del	NP_065202.2:n.*301_*304del
NM_020469.3:c.*301_*304del	NP_065202.2:n.*301_*304del