Canonical Allele Identifier: CA2692330371

Gene: ABO

Linked Data

• gnomAD v4: 9-133256380-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256385del , CM000671.2:g.133256385del	GRCh38
NC_000009.11:g.136131772del , CM000671.1:g.136131772del	GRCh37
NC_000009.10:g.135121593del	NCBI36
NG_006669.1:g.21287del
NG_006669.2:g.23835del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.404-25del
ENST00000647353.1:n.54-5229del
ENST00000651471.1:n.330-25del
ENST00000679909.1:c.28+18781del	ENSP00000506089.1:n.28+18781del
ENST00000453660.3:n.386-25del
ENST00000538324.2:c.372-25del	ENSP00000483018.1:n.372-25del
ENST00000611156.4:c.372-25del	ENSP00000483265.1:n.372-25del
NM_020469.2:c.375-25del	NP_065202.2:n.375-25del
NM_020469.3:c.375-25del	NP_065202.2:n.375-25del