Canonical Allele Identifier: CA1882578988
Gene: ABO HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255578A= , CM000671.2:g.133255578A= GRCh38
NC_000009.11:g.136130965A= , CM000671.1:g.136130965A= GRCh37
NC_000009.10:g.135120786A= NCBI36
NG_006669.1:g.22090T=
NG_006669.2:g.24638T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1182T=
ENST00000647353.1:n.54-4426T=
ENST00000679909.1:c.28+19584T= ENSP00000506089.1:n.28+19584T=
ENST00000453660.3:n.1164T=
ENST00000611156.4:c.*88T= ENSP00000483265.1:n.*88T=
NM_020469.2:c.*88T= NP_065202.2:n.*88T=
NM_020469.3:c.*88T= NP_065202.2:n.*88T=
Search 100 bp 5'
Search 100 bp 3'