Canonical Allele Identifier: CA1882584465
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260361A= , CM000671.2:g.133260361A= GRCh38
NC_000009.11:g.136135764A= , CM000671.1:g.136135764A= GRCh37
NC_000009.10:g.135125585A= NCBI36
NG_006669.1:g.17289T=
NG_006669.2:g.19854T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.186-495T=
ENST00000647353.1:n.54-9209T=
ENST00000651471.1:n.191-495T=
ENST00000679909.1:c.28+14801T= ENSP00000506089.1:n.28+14801T=
ENST00000453660.3:n.168-495T=
ENST00000538324.2:c.156-495T= ENSP00000483018.1:n.156-495T=
ENST00000611156.4:c.156-495T= ENSP00000483265.1:n.156-495T=
NM_020469.2:c.156-495T= NP_065202.2:n.156-495T=
NM_020469.3:c.156-495T= NP_065202.2:n.156-495T=