Canonical Allele Identifier: CA860763746

Gene: ABO

Linked Data

• dbSNP Id: rs1442272000
• gnomAD v3: 9-133274265-C-T
• gnomAD v4: 9-133274265-C-T
• MyVariant Identifiers: chr9:g.133274265C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133274265C>T , CM000671.2:g.133274265C>T	GRCh38
NC_000009.11:g.136149681C>T , CM000671.1:g.136149681C>T	GRCh37
NC_000009.10:g.135139502C>T	NCBI36
NG_006669.1:g.3370G>A
NG_006669.2:g.5950G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.58+897G>A
ENST00000647353.1:n.53+897G>A
ENST00000651471.1:n.63+1697G>A
ENST00000679909.1:c.28+897G>A	ENSP00000506089.1:n.28+897G>A
ENST00000453660.3:n.40+897G>A
ENST00000538324.2:c.28+897G>A	ENSP00000483018.1:n.28+897G>A
ENST00000611156.4:c.28+897G>A	ENSP00000483265.1:n.28+897G>A
NM_020469.2:c.28+897G>A	NP_065202.2:n.28+897G>A
NM_020469.3:c.28+897G>A	NP_065202.2:n.28+897G>A