Canonical Allele Identifier: CA375686897
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258134T>G , CM000671.2:g.133258134T>G GRCh38
NC_000009.11:g.136133524T>G , CM000671.1:g.136133524T>G GRCh37
NC_000009.10:g.135123345T>G NCBI36
NG_006669.1:g.19530A>C
NG_006669.2:g.22081A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-2A>C
ENST00000647353.1:n.54-6982A>C
ENST00000651471.1:n.239-2A>C
ENST00000679909.1:c.28+17028A>C ENSP00000506089.1:n.28+17028A>C
ENST00000453660.3:n.216-2A>C
ENST00000538324.2:c.204-2A>C ENSP00000483018.1:n.204-2A>C
ENST00000611156.4:c.204-2A>C ENSP00000483265.1:n.204-2A>C
NM_020469.2:c.204-2A>C NP_065202.2:n.204-2A>C
NM_020469.3:c.204-2A>C NP_065202.2:n.204-2A>C