Canonical Allele Identifier: CA1882582934
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257993C= , CM000671.2:g.133257993C= GRCh38
NG_006669.2:g.22222G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.269+104G=
ENST00000647353.1:n.54-6841G=
ENST00000651471.1:n.329+49G=
ENST00000679909.1:c.28+17169G= ENSP00000506089.1:n.28+17169G=
ENST00000453660.3:n.251+104G=
ENST00000538324.2:c.239+104G= ENSP00000483018.1:n.239+104G=
ENST00000611156.4:c.239+104G= ENSP00000483265.1:n.239+104G=
NM_020469.2:c.239+104G= NP_065202.2:n.239+104G=
NM_020469.3:c.239+104G= NP_065202.2:n.239+104G=