Canonical Allele Identifier: CA1882583486
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258403A= , CM000671.2:g.133258403A= GRCh38
NC_000009.11:g.136133794A= , CM000671.1:g.136133794A= GRCh37
NC_000009.10:g.135123615A= NCBI36
NG_006669.1:g.19260T=
NG_006669.2:g.21812T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-271T=
ENST00000647353.1:n.54-7251T=
ENST00000651471.1:n.239-271T=
ENST00000679909.1:c.28+16759T= ENSP00000506089.1:n.28+16759T=
ENST00000453660.3:n.216-271T=
ENST00000538324.2:c.204-271T= ENSP00000483018.1:n.204-271T=
ENST00000611156.4:c.204-271T= ENSP00000483265.1:n.204-271T=
NM_020469.2:c.204-271T= NP_065202.2:n.204-271T=
NM_020469.3:c.204-271T= NP_065202.2:n.204-271T=