Canonical Allele Identifier: CA1882585082
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1834715386
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133261764T>C , CM000671.2:g.133261764T>C GRCh38
NC_000009.11:g.136137167T>C , CM000671.1:g.136137167T>C GRCh37
NC_000009.10:g.135126988T>C NCBI36
NG_006669.1:g.15886A>G
NG_006669.2:g.18451A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.128+335A>G
ENST00000647353.1:n.54-10612A>G
ENST00000651471.1:n.133+335A>G
ENST00000679909.1:c.28+13398A>G ENSP00000506089.1:n.28+13398A>G
ENST00000453660.3:n.110+335A>G
ENST00000538324.2:c.98+335A>G ENSP00000483018.1:n.98+335A>G
ENST00000611156.4:c.98+335A>G ENSP00000483265.1:n.98+335A>G
NM_020469.2:c.98+335A>G NP_065202.2:n.98+335A>G
NM_020469.3:c.98+335A>G NP_065202.2:n.98+335A>G
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