Canonical Allele Identifier: CA200770760

Gene: ABO

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133273232C>T , CM000671.2:g.133273232C>T	GRCh38
NG_006669.1:g.4404G>A
NG_006669.2:g.6983G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.58+1930G>A
ENST00000647353.1:n.53+1930G>A
ENST00000651471.1:n.63+2730G>A
ENST00000679909.1:c.28+1930G>A	ENSP00000506089.1:n.28+1930G>A
ENST00000453660.3:n.40+1930G>A
ENST00000538324.2:c.28+1930G>A	ENSP00000483018.1:n.28+1930G>A
ENST00000611156.4:c.28+1930G>A	ENSP00000483265.1:n.28+1930G>A
NM_020469.2:c.28+1930G>A	NP_065202.2:n.28+1930G>A
NM_020469.3:c.28+1930G>A	NP_065202.2:n.28+1930G>A