Canonical Allele Identifier: CA467780618
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1467726194
gnomAD v3: 9-133255417-T-C
gnomAD v4: 9-133255417-T-C
MyVariant Identifiers: chr9:g.136130804T>C (hg19) chr9:g.133255417T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255417T>C , CM000671.2:g.133255417T>C GRCh38
NC_000009.11:g.136130804T>C , CM000671.1:g.136130804T>C GRCh37
NC_000009.10:g.135120625T>C NCBI36
NG_006669.1:g.22251A>G
NG_006669.2:g.24799A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1343A>G
ENST00000647353.1:n.54-4265A>G
ENST00000679909.1:c.28+19745A>G ENSP00000506089.1:n.28+19745A>G
ENST00000453660.3:n.1325A>G
ENST00000611156.4:c.*249A>G ENSP00000483265.1:n.*249A>G
NM_020469.2:c.*249A>G NP_065202.2:n.*249A>G
NM_020469.3:c.*249A>G NP_065202.2:n.*249A>G
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