Canonical Allele Identifier: CA1882578571
Gene: ABO HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255381T= , CM000671.2:g.133255381T= GRCh38
NC_000009.11:g.136130768T= , CM000671.1:g.136130768T= GRCh37
NC_000009.10:g.135120589T= NCBI36
NG_006669.1:g.22287A=
NG_006669.2:g.24835A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1379A=
ENST00000647353.1:n.54-4229A=
ENST00000679909.1:c.28+19781A= ENSP00000506089.1:n.28+19781A=
ENST00000453660.3:n.1361A=
ENST00000611156.4:c.*285A= ENSP00000483265.1:n.*285A=
NM_020469.2:c.*285A= NP_065202.2:n.*285A=
NM_020469.3:c.*285A= NP_065202.2:n.*285A=
Search 100 bp 5'
Search 100 bp 3'