Canonical Allele Identifier: CA2580907997
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260074G>C , CM000671.2:g.133260074G>C GRCh38
NG_006669.1:g.17576C>G
NG_006669.2:g.20141C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.186-208C>G
ENST00000647353.1:n.54-8922C>G
ENST00000651471.1:n.191-208C>G
ENST00000679909.1:c.28+15088C>G ENSP00000506089.1:n.28+15088C>G
ENST00000453660.3:n.168-208C>G
ENST00000538324.2:c.156-208C>G ENSP00000483018.1:n.156-208C>G
ENST00000611156.4:c.156-208C>G ENSP00000483265.1:n.156-208C>G
NM_020469.2:c.156-208C>G NP_065202.2:n.156-208C>G
NM_020469.3:c.156-208C>G NP_065202.2:n.156-208C>G
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