Canonical Allele Identifier: CA591309051
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1299319727

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257246_133257247del , CM000671.2:g.133257246_133257247del GRCh38
NC_000009.11:g.136132633_136132634del , CM000671.1:g.136132633_136132634del GRCh37
NC_000009.10:g.135122454_135122455del NCBI36
NG_006669.1:g.20421_20422del

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+162_403+163del
ENST00000647353.1:n.54-6095_54-6094del
ENST00000651471.1:n.329+795_329+796del
ENST00000679909.1:c.28+17915_28+17916del ENSP00000506089.1:n.28+17915_28+17916del
ENST00000453660.3:n.385+162_385+163del
ENST00000538324.2:c.371+162_371+163del ENSP00000483018.1:n.371+162_371+163del
ENST00000611156.4:c.371+162_371+163del ENSP00000483265.1:n.371+162_371+163del
NM_020469.2:c.374+162_374+163del NP_065202.2:n.374+162_374+163del
NM_020469.3:c.374+162_374+163del NP_065202.2:n.374+162_374+163del