Canonical Allele Identifier: CA1882582449
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257537T= , CM000671.2:g.133257537T= GRCh38
NC_000009.11:g.136132924T= , CM000671.1:g.136132924T= GRCh37
NC_000009.10:g.135122745T= NCBI36
NG_006669.1:g.20130A=
NG_006669.2:g.22678A=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.275A=
ENST00000647353.1:n.54-6385A=
ENST00000651471.1:n.329+505A=
ENST00000679909.1:c.28+17625A= ENSP00000506089.1:n.28+17625A=
ENST00000453660.3:n.257A=
ENST00000538324.2:c.245A= ENSP00000483018.1:p.Lys82=
ENST00000611156.4:c.245A= ENSP00000483265.1:p.Lys82=
NM_020469.2:c.245A= NP_065202.2:p.Lys82=
NM_020469.3:c.245A= NP_065202.2:p.Lys82=