Canonical Allele Identifier: CA2786163438
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260081A>G , CM000671.2:g.133260081A>G GRCh38
NC_000009.11:g.136135485A>G , CM000671.1:g.136135485A>G GRCh37
NC_000009.10:g.135125306A>G NCBI36
NG_006669.1:g.17569T>C
NG_006669.2:g.20134T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.186-215T>C
ENST00000647353.1:n.54-8929T>C
ENST00000651471.1:n.191-215T>C
ENST00000679909.1:c.28+15081T>C ENSP00000506089.1:n.28+15081T>C
ENST00000453660.3:n.168-215T>C
ENST00000538324.2:c.156-215T>C ENSP00000483018.1:n.156-215T>C
ENST00000611156.4:c.156-215T>C ENSP00000483265.1:n.156-215T>C
NM_020469.2:c.156-215T>C NP_065202.2:n.156-215T>C
NM_020469.3:c.156-215T>C NP_065202.2:n.156-215T>C
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