Canonical Allele Identifier: CA1882582989
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258056C= , CM000671.2:g.133258056C= GRCh38
NC_000009.11:g.136133446C= , CM000671.1:g.136133446C= GRCh37
NC_000009.10:g.135123267C= NCBI36
NG_006669.1:g.19608G=
NG_006669.2:g.22159G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.269+41G=
ENST00000647353.1:n.54-6904G=
ENST00000651471.1:n.315G=
ENST00000679909.1:c.28+17106G= ENSP00000506089.1:n.28+17106G=
ENST00000453660.3:n.251+41G=
ENST00000538324.2:c.239+41G= ENSP00000483018.1:n.239+41G=
ENST00000611156.4:c.239+41G= ENSP00000483265.1:n.239+41G=
NM_020469.2:c.239+41G= NP_065202.2:n.239+41G=
NM_020469.3:c.239+41G= NP_065202.2:n.239+41G=