Canonical Allele Identifier: CA1882582872
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1834632092
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257898G>T , CM000671.2:g.133257898G>T GRCh38
NC_000009.11:g.136133285G>T , CM000671.1:g.136133285G>T GRCh37
NC_000009.10:g.135123106G>T NCBI36
NG_006669.1:g.19769C>A
NG_006669.2:g.22317C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.269+199C>A
ENST00000647353.1:n.54-6746C>A
ENST00000651471.1:n.329+144C>A
ENST00000679909.1:c.28+17264C>A ENSP00000506089.1:n.28+17264C>A
ENST00000453660.3:n.251+199C>A
ENST00000538324.2:c.239+199C>A ENSP00000483018.1:n.239+199C>A
ENST00000611156.4:c.239+199C>A ENSP00000483265.1:n.239+199C>A
NM_020469.2:c.239+199C>A NP_065202.2:n.239+199C>A
NM_020469.3:c.239+199C>A NP_065202.2:n.239+199C>A
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