Canonical Allele Identifier: CA200764876
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs7469764
gnomAD v3: 9-133255376-T-G
gnomAD v4: 9-133255376-T-G
MyVariant Identifiers: chr9:g.136130763T>G (hg19) chr9:g.133255376T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255376T>G , CM000671.2:g.133255376T>G GRCh38
NC_000009.11:g.136130763T>G , CM000671.1:g.136130763T>G GRCh37
NC_000009.10:g.135120584T>G NCBI36
NG_006669.1:g.22292A>C
NG_006669.2:g.24840A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1384A>C
ENST00000647353.1:n.54-4224A>C
ENST00000679909.1:c.28+19786A>C ENSP00000506089.1:n.28+19786A>C
ENST00000453660.3:n.1366A>C
ENST00000611156.4:c.*290A>C ENSP00000483265.1:n.*290A>C
NM_020469.2:c.*290A>C NP_065202.2:n.*290A>C
NM_020469.3:c.*290A>C NP_065202.2:n.*290A>C
Search 100 bp 5'
Search 100 bp 3'