Canonical Allele Identifier: CA2580908009
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133261737G>C , CM000671.2:g.133261737G>C GRCh38
NC_000009.11:g.136137140G>C , CM000671.1:g.136137140G>C GRCh37
NC_000009.10:g.135126961G>C NCBI36
NG_006669.1:g.15913C>G
NG_006669.2:g.18478C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.129-363C>G
ENST00000647353.1:n.54-10585C>G
ENST00000651471.1:n.134-363C>G
ENST00000679909.1:c.28+13425C>G ENSP00000506089.1:n.28+13425C>G
ENST00000453660.3:n.111-363C>G
ENST00000538324.2:c.99-363C>G ENSP00000483018.1:n.99-363C>G
ENST00000611156.4:c.99-363C>G ENSP00000483265.1:n.99-363C>G
NM_020469.2:c.99-363C>G NP_065202.2:n.99-363C>G
NM_020469.3:c.99-363C>G NP_065202.2:n.99-363C>G
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