Canonical Allele Identifier: CA1129716394

Gene: ABO

Linked Data

• dbSNP Id: rs1834640308
• gnomAD v3: 9-133258329-CAG-C
• gnomAD v4: 9-133258329-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258332_133258333del , CM000671.2:g.133258332_133258333del	GRCh38
NC_000009.11:g.136133723_136133724del , CM000671.1:g.136133723_136133724del	GRCh37
NC_000009.10:g.135123544_135123545del	NCBI36
NG_006669.1:g.19332_19333del
NG_006669.2:g.21884_21885del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.234-199_234-198del
ENST00000647353.1:n.54-7179_54-7178del
ENST00000651471.1:n.239-199_239-198del
ENST00000679909.1:c.28+16831_28+16832del	ENSP00000506089.1:n.28+16831_28+16832del
ENST00000453660.3:n.216-199_216-198del
ENST00000538324.2:c.204-199_204-198del	ENSP00000483018.1:n.204-199_204-198del
ENST00000611156.4:c.204-199_204-198del	ENSP00000483265.1:n.204-199_204-198del
NM_020469.2:c.204-199_204-198del	NP_065202.2:n.204-199_204-198del
NM_020469.3:c.204-199_204-198del	NP_065202.2:n.204-199_204-198del