Canonical Allele Identifier: CA1882590528
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1834957349
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274070A>C , CM000671.2:g.133274070A>C GRCh38
NC_000009.11:g.136149486A>C , CM000671.1:g.136149486A>C GRCh37
NC_000009.10:g.135139307A>C NCBI36
NG_006669.1:g.3565T>G
NG_006669.2:g.6145T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+1092T>G
ENST00000647353.1:n.53+1092T>G
ENST00000651471.1:n.63+1892T>G
ENST00000679909.1:c.28+1092T>G ENSP00000506089.1:n.28+1092T>G
ENST00000453660.3:n.40+1092T>G
ENST00000538324.2:c.28+1092T>G ENSP00000483018.1:n.28+1092T>G
ENST00000611156.4:c.28+1092T>G ENSP00000483265.1:n.28+1092T>G
NM_020469.2:c.28+1092T>G NP_065202.2:n.28+1092T>G
NM_020469.3:c.28+1092T>G NP_065202.2:n.28+1092T>G
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