Canonical Allele Identifier: CA2954284612
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256185dup , CM000671.2:g.133256185dup GRCh38
NC_000009.11:g.136131572dup , CM000671.1:g.136131572dup GRCh37
NC_000009.10:g.135121393dup NCBI36
NG_006669.1:g.21484dup
NG_006669.2:g.24032dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.576dup
ENST00000647353.1:n.54-5032dup
ENST00000651471.1:n.502dup
ENST00000679909.1:c.28+18978dup ENSP00000506089.1:n.28+18978dup
ENST00000453660.3:n.558dup
ENST00000538324.2:c.544dup ENSP00000483018.1:p.Asp182GlyfsTer12
ENST00000611156.4:c.544dup ENSP00000483265.1:p.Asp182GlyfsTer12
NM_020469.2:c.547dup NP_065202.2:p.Asp183GlyfsTer12
NM_020469.3:c.547dup NP_065202.2:p.Asp183GlyfsTer12