Canonical Allele Identifier: CA860755298

Gene: ABO

Linked Data

• dbSNP Id: rs8176712
• gnomAD v3: 9-133258192-A-AG
• gnomAD v4: 9-133258192-A-AG
• MyVariant Identifiers: chr9:g.133258192_133258193insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258196dup , CM000671.2:g.133258196dup	GRCh38
NC_000009.11:g.136133587dup , CM000671.1:g.136133587dup	GRCh37
NC_000009.10:g.135123408dup	NCBI36
NG_006669.1:g.19470dup
NG_006669.2:g.22022dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.234-61dup
ENST00000647353.1:n.54-7041dup
ENST00000651471.1:n.239-61dup
ENST00000679909.1:c.28+16969dup	ENSP00000506089.1:n.28+16969dup
ENST00000453660.3:n.216-61dup
ENST00000538324.2:c.204-61dup	ENSP00000483018.1:n.204-61dup
ENST00000611156.4:c.204-61dup	ENSP00000483265.1:n.204-61dup
NM_020469.2:c.204-61dup	NP_065202.2:n.204-61dup
NM_020469.3:c.204-61dup	NP_065202.2:n.204-61dup