Canonical Allele Identifier: CA1882590606
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274220T= , CM000671.2:g.133274220T= GRCh38
NC_000009.11:g.136149636T= , CM000671.1:g.136149636T= GRCh37
NC_000009.10:g.135139457T= NCBI36
NG_006669.1:g.3415A=
NG_006669.2:g.5995A=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+942A=
ENST00000647353.1:n.53+942A=
ENST00000651471.1:n.63+1742A=
ENST00000679909.1:c.28+942A= ENSP00000506089.1:n.28+942A=
ENST00000453660.3:n.40+942A=
ENST00000538324.2:c.28+942A= ENSP00000483018.1:n.28+942A=
ENST00000611156.4:c.28+942A= ENSP00000483265.1:n.28+942A=
NM_020469.2:c.28+942A= NP_065202.2:n.28+942A=
NM_020469.3:c.28+942A= NP_065202.2:n.28+942A=