Canonical Allele Identifier: CA2692330336

Gene: ABO

Linked Data

• gnomAD v4: 9-133255596-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255598dup , CM000671.2:g.133255598dup	GRCh38
NC_000009.11:g.136130985dup , CM000671.1:g.136130985dup	GRCh37
NC_000009.10:g.135120806dup	NCBI36
NG_006669.1:g.22071dup
NG_006669.2:g.24619dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1163dup
ENST00000647353.1:n.54-4445dup
ENST00000679909.1:c.28+19565dup	ENSP00000506089.1:n.28+19565dup
ENST00000453660.3:n.1145dup
ENST00000611156.4:c.*69dup	ENSP00000483265.1:n.*69dup
NM_020469.2:c.*69dup	NP_065202.2:n.*69dup
NM_020469.3:c.*69dup	NP_065202.2:n.*69dup