Canonical Allele Identifier: CA200766045
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs149320846

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257340del , CM000671.2:g.133257340del GRCh38
NC_000009.11:g.136132727del , CM000671.1:g.136132727del GRCh37
NC_000009.10:g.135122548del NCBI36
NG_006669.1:g.20328del
NG_006669.2:g.22876del

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+69del
ENST00000647353.1:n.54-6188del
ENST00000651471.1:n.329+702del
ENST00000679909.1:c.28+17822del ENSP00000506089.1:n.28+17822del
ENST00000453660.3:n.385+69del
ENST00000538324.2:c.371+69del ENSP00000483018.1:n.371+69del
ENST00000611156.4:c.371+69del ENSP00000483265.1:n.371+69del
NM_020469.2:c.374+69del NP_065202.2:n.374+69del
NM_020469.3:c.374+69del NP_065202.2:n.374+69del