Canonical Allele Identifier: CA860760225

Gene: ABO

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133266790C>T , CM000671.2:g.133266790C>T	GRCh38
NG_006669.2:g.13425G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.59-4622G>A
ENST00000647353.1:n.53+8372G>A
ENST00000651471.1:n.64-4622G>A
ENST00000679909.1:c.28+8372G>A	ENSP00000506089.1:n.28+8372G>A
ENST00000453660.3:n.41-4622G>A
ENST00000538324.2:c.29-4622G>A	ENSP00000483018.1:n.29-4622G>A
ENST00000611156.4:c.29-4622G>A	ENSP00000483265.1:n.29-4622G>A
NM_020469.2:c.29-4622G>A	NP_065202.2:n.29-4622G>A
NM_020469.3:c.29-4622G>A	NP_065202.2:n.29-4622G>A