Canonical Allele Identifier: CA200767711

Gene: ABO

Linked Data

• dbSNP Id: rs896068290
• gnomAD v3: 9-133261779-G-A
• gnomAD v4: 9-133261779-G-A
• MyVariant Identifiers: chr9:g.133261779G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133261779G>A , CM000671.2:g.133261779G>A	GRCh38
NC_000009.11:g.136137182G>A , CM000671.1:g.136137182G>A	GRCh37
NC_000009.10:g.135127003G>A	NCBI36
NG_006669.1:g.15871C>T
NG_006669.2:g.18436C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.128+320C>T
ENST00000647353.1:n.54-10627C>T
ENST00000651471.1:n.133+320C>T
ENST00000679909.1:c.28+13383C>T	ENSP00000506089.1:n.28+13383C>T
ENST00000453660.3:n.110+320C>T
ENST00000538324.2:c.98+320C>T	ENSP00000483018.1:n.98+320C>T
ENST00000611156.4:c.98+320C>T	ENSP00000483265.1:n.98+320C>T
NM_020469.2:c.98+320C>T	NP_065202.2:n.98+320C>T
NM_020469.3:c.98+320C>T	NP_065202.2:n.98+320C>T