Canonical Allele Identifier: CA467784357
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs782544052
MyVariant Identifiers: chr9:g.136135760G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260357G>T , CM000671.2:g.133260357G>T GRCh38
NC_000009.11:g.136135760G>T , CM000671.1:g.136135760G>T GRCh37
NC_000009.10:g.135125581G>T NCBI36
NG_006669.1:g.17293C>A
NG_006669.2:g.19858C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.186-491C>A
ENST00000647353.1:n.54-9205C>A
ENST00000651471.1:n.191-491C>A
ENST00000679909.1:c.28+14805C>A ENSP00000506089.1:n.28+14805C>A
ENST00000453660.3:n.168-491C>A
ENST00000538324.2:c.156-491C>A ENSP00000483018.1:n.156-491C>A
ENST00000611156.4:c.156-491C>A ENSP00000483265.1:n.156-491C>A
NM_020469.2:c.156-491C>A NP_065202.2:n.156-491C>A
NM_020469.3:c.156-491C>A NP_065202.2:n.156-491C>A
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