Canonical Allele Identifier: CA2692330920
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258261del , CM000671.2:g.133258261del GRCh38
NC_000009.11:g.136133652del , CM000671.1:g.136133652del GRCh37
NC_000009.10:g.135123473del NCBI36
NG_006669.1:g.19403del
NG_006669.2:g.21955del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-128del
ENST00000647353.1:n.54-7108del
ENST00000651471.1:n.239-128del
ENST00000679909.1:c.28+16902del ENSP00000506089.1:n.28+16902del
ENST00000453660.3:n.216-128del
ENST00000538324.2:c.204-128del ENSP00000483018.1:n.204-128del
ENST00000611156.4:c.204-128del ENSP00000483265.1:n.204-128del
NM_020469.2:c.204-128del NP_065202.2:n.204-128del
NM_020469.3:c.204-128del NP_065202.2:n.204-128del