Canonical Allele Identifier: CA200767336
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs5901011

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260286dup , CM000671.2:g.133260286dup GRCh38
NG_006669.1:g.17368dup
NG_006669.2:g.19933dup

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.186-416dup
ENST00000647353.1:n.54-9130dup
ENST00000651471.1:n.191-416dup
ENST00000679909.1:c.28+14880dup ENSP00000506089.1:n.28+14880dup
ENST00000453660.3:n.168-416dup
ENST00000538324.2:c.156-416dup ENSP00000483018.1:n.156-416dup
ENST00000611156.4:c.156-416dup ENSP00000483265.1:n.156-416dup
NM_020469.2:c.156-416dup NP_065202.2:n.156-416dup
NM_020469.3:c.156-416dup NP_065202.2:n.156-416dup