Canonical Allele Identifier: CA1882578561
Gene: ABO HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255376T= , CM000671.2:g.133255376T= GRCh38
NC_000009.11:g.136130763T= , CM000671.1:g.136130763T= GRCh37
NC_000009.10:g.135120584T= NCBI36
NG_006669.1:g.22292A=
NG_006669.2:g.24840A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1384A=
ENST00000647353.1:n.54-4224A=
ENST00000679909.1:c.28+19786A= ENSP00000506089.1:n.28+19786A=
ENST00000453660.3:n.1366A=
ENST00000611156.4:c.*290A= ENSP00000483265.1:n.*290A=
NM_020469.2:c.*290A= NP_065202.2:n.*290A=
NM_020469.3:c.*290A= NP_065202.2:n.*290A=
Search 100 bp 5'
Search 100 bp 3'