Canonical Allele Identifier: CA860756128
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1410162633
gnomAD v3: 9-133260056-C-T
gnomAD v4: 9-133260056-C-T
MyVariant Identifiers: chr9:g.133260056C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260056C>T , CM000671.2:g.133260056C>T GRCh38
NC_000009.11:g.136135460C>T , CM000671.1:g.136135460C>T GRCh37
NC_000009.10:g.135125281C>T NCBI36
NG_006669.1:g.17594G>A
NG_006669.2:g.20159G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.186-190G>A
ENST00000647353.1:n.54-8904G>A
ENST00000651471.1:n.191-190G>A
ENST00000679909.1:c.28+15106G>A ENSP00000506089.1:n.28+15106G>A
ENST00000453660.3:n.168-190G>A
ENST00000538324.2:c.156-190G>A ENSP00000483018.1:n.156-190G>A
ENST00000611156.4:c.156-190G>A ENSP00000483265.1:n.156-190G>A
NM_020469.2:c.156-190G>A NP_065202.2:n.156-190G>A
NM_020469.3:c.156-190G>A NP_065202.2:n.156-190G>A
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