Canonical Allele Identifier: CA860754287
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1317602320

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257220_133257227dup , CM000671.2:g.133257220_133257227dup GRCh38
NC_000009.11:g.136132607_136132614dup , CM000671.1:g.136132607_136132614dup GRCh37
NC_000009.10:g.135122428_135122435dup NCBI36
NG_006669.1:g.20441_20448dup
NG_006669.2:g.22989_22996dup

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+182_403+189dup
ENST00000647353.1:n.54-6075_54-6068dup
ENST00000651471.1:n.329+815_329+822dup
ENST00000679909.1:c.28+17935_28+17942dup ENSP00000506089.1:n.28+17935_28+17942dup
ENST00000453660.3:n.385+182_385+189dup
ENST00000538324.2:c.371+182_371+189dup ENSP00000483018.1:n.371+182_371+189dup
ENST00000611156.4:c.371+182_371+189dup ENSP00000483265.1:n.371+182_371+189dup
NM_020469.2:c.374+182_374+189dup NP_065202.2:n.374+182_374+189dup
NM_020469.3:c.374+182_374+189dup NP_065202.2:n.374+182_374+189dup