Canonical Allele Identifier: CA1882584421
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1305455811
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260237T>A , CM000671.2:g.133260237T>A GRCh38
NC_000009.11:g.136135641T>A , CM000671.1:g.136135641T>A GRCh37
NC_000009.10:g.135125462T>A NCBI36
NG_006669.1:g.17413A>T
NG_006669.2:g.19978A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.186-371A>T
ENST00000647353.1:n.54-9085A>T
ENST00000651471.1:n.191-371A>T
ENST00000679909.1:c.28+14925A>T ENSP00000506089.1:n.28+14925A>T
ENST00000453660.3:n.168-371A>T
ENST00000538324.2:c.156-371A>T ENSP00000483018.1:n.156-371A>T
ENST00000611156.4:c.156-371A>T ENSP00000483265.1:n.156-371A>T
NM_020469.2:c.156-371A>T NP_065202.2:n.156-371A>T
NM_020469.3:c.156-371A>T NP_065202.2:n.156-371A>T
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