Canonical Allele Identifier: CA591309669

Gene: ABO

Linked Data

• dbSNP Id: rs1554758025
• gnomAD v2: 9-136135497-A-G
• gnomAD v3: 9-133260093-A-G
• gnomAD v4: 9-133260093-A-G
• MyVariant Identifiers: chr9:g.136135497A>G (hg19) ; chr9:g.133260093A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133260093A>G , CM000671.2:g.133260093A>G	GRCh38
NC_000009.11:g.136135497A>G , CM000671.1:g.136135497A>G	GRCh37
NC_000009.10:g.135125318A>G	NCBI36
NG_006669.1:g.17557T>C
NG_006669.2:g.20122T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.186-227T>C
ENST00000647353.1:n.54-8941T>C
ENST00000651471.1:n.191-227T>C
ENST00000679909.1:c.28+15069T>C	ENSP00000506089.1:n.28+15069T>C
ENST00000453660.3:n.168-227T>C
ENST00000538324.2:c.156-227T>C	ENSP00000483018.1:n.156-227T>C
ENST00000611156.4:c.156-227T>C	ENSP00000483265.1:n.156-227T>C
NM_020469.2:c.156-227T>C	NP_065202.2:n.156-227T>C
NM_020469.3:c.156-227T>C	NP_065202.2:n.156-227T>C