Canonical Allele Identifier: CA2692331602
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133262054C>G , CM000671.2:g.133262054C>G GRCh38
NC_000009.11:g.136137457C>G , CM000671.1:g.136137457C>G GRCh37
NC_000009.10:g.135127278C>G NCBI36
NG_006669.1:g.15595G>C
NG_006669.2:g.18161G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.128+45G>C
ENST00000647353.1:n.54-10902G>C
ENST00000651471.1:n.133+45G>C
ENST00000679909.1:c.28+13108G>C ENSP00000506089.1:n.28+13108G>C
ENST00000453660.3:n.110+45G>C
ENST00000538324.2:c.98+45G>C ENSP00000483018.1:n.98+45G>C
ENST00000611156.4:c.98+45G>C ENSP00000483265.1:n.98+45G>C
NM_020469.2:c.98+45G>C NP_065202.2:n.98+45G>C
NM_020469.3:c.98+45G>C NP_065202.2:n.98+45G>C