Canonical Allele Identifier: CA860756163

Gene: ABO

Linked Data

• dbSNP Id: rs1159353542
• gnomAD v3: 9-133260138-A-C
• gnomAD v4: 9-133260138-A-C
• MyVariant Identifiers: chr9:g.133260138A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133260138A>C , CM000671.2:g.133260138A>C	GRCh38
NC_000009.11:g.136135542A>C , CM000671.1:g.136135542A>C	GRCh37
NC_000009.10:g.135125363A>C	NCBI36
NG_006669.1:g.17512T>G
NG_006669.2:g.20077T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.186-272T>G
ENST00000647353.1:n.54-8986T>G
ENST00000651471.1:n.191-272T>G
ENST00000679909.1:c.28+15024T>G	ENSP00000506089.1:n.28+15024T>G
ENST00000453660.3:n.168-272T>G
ENST00000538324.2:c.156-272T>G	ENSP00000483018.1:n.156-272T>G
ENST00000611156.4:c.156-272T>G	ENSP00000483265.1:n.156-272T>G
NM_020469.2:c.156-272T>G	NP_065202.2:n.156-272T>G
NM_020469.3:c.156-272T>G	NP_065202.2:n.156-272T>G