Canonical Allele Identifier: CA1882578779
Gene: ABO HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255458G= , CM000671.2:g.133255458G= GRCh38
NC_000009.11:g.136130845G= , CM000671.1:g.136130845G= GRCh37
NC_000009.10:g.135120666G= NCBI36
NG_006669.1:g.22210C=
NG_006669.2:g.24758C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1302C=
ENST00000647353.1:n.54-4306C=
ENST00000679909.1:c.28+19704C= ENSP00000506089.1:n.28+19704C=
ENST00000453660.3:n.1284C=
ENST00000611156.4:c.*208C= ENSP00000483265.1:n.*208C=
NM_020469.2:c.*208C= NP_065202.2:n.*208C=
NM_020469.3:c.*208C= NP_065202.2:n.*208C=
Search 100 bp 5'
Search 100 bp 3'