Canonical Allele Identifier: CA2786163442
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260215G>A , CM000671.2:g.133260215G>A GRCh38
NC_000009.11:g.136135619G>A , CM000671.1:g.136135619G>A GRCh37
NC_000009.10:g.135125440G>A NCBI36
NG_006669.1:g.17435C>T
NG_006669.2:g.20000C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.186-349C>T
ENST00000647353.1:n.54-9063C>T
ENST00000651471.1:n.191-349C>T
ENST00000679909.1:c.28+14947C>T ENSP00000506089.1:n.28+14947C>T
ENST00000453660.3:n.168-349C>T
ENST00000538324.2:c.156-349C>T ENSP00000483018.1:n.156-349C>T
ENST00000611156.4:c.156-349C>T ENSP00000483265.1:n.156-349C>T
NM_020469.2:c.156-349C>T NP_065202.2:n.156-349C>T
NM_020469.3:c.156-349C>T NP_065202.2:n.156-349C>T
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