Canonical Allele Identifier: CA2786163349
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258167dup , CM000671.2:g.133258167dup GRCh38
NC_000009.11:g.136133557dup , CM000671.1:g.136133557dup GRCh37
NC_000009.10:g.135123378dup NCBI36
NG_006669.1:g.19497dup
NG_006669.2:g.22048dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-35dup
ENST00000647353.1:n.54-7015dup
ENST00000651471.1:n.239-35dup
ENST00000679909.1:c.28+16995dup ENSP00000506089.1:n.28+16995dup
ENST00000453660.3:n.216-35dup
ENST00000538324.2:c.204-35dup ENSP00000483018.1:n.204-35dup
ENST00000611156.4:c.204-35dup ENSP00000483265.1:n.204-35dup
NM_020469.2:c.204-35dup NP_065202.2:n.204-35dup
NM_020469.3:c.204-35dup NP_065202.2:n.204-35dup