Canonical Allele Identifier: CA2692330841

Gene: ABO

Linked Data

• gnomAD v4: 9-133258191-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258191_133258192insG , CM000671.2:g.133258191_133258192insG	GRCh38
NG_006669.2:g.22023_22024insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.234-60_234-59insC
ENST00000647353.1:n.54-7040_54-7039insC
ENST00000651471.1:n.239-60_239-59insC
ENST00000679909.1:c.28+16970_28+16971insC	ENSP00000506089.1:n.28+16970_28+16971insC
ENST00000453660.3:n.216-60_216-59insC
ENST00000538324.2:c.204-60_204-59insC	ENSP00000483018.1:n.204-60_204-59insC
ENST00000611156.4:c.204-60_204-59insC	ENSP00000483265.1:n.204-60_204-59insC
NM_020469.2:c.204-60_204-59insC	NP_065202.2:n.204-60_204-59insC
NM_020469.3:c.204-60_204-59insC	NP_065202.2:n.204-60_204-59insC