Canonical Allele Identifier: CA1882582247
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257368C= , CM000671.2:g.133257368C= GRCh38
NC_000009.11:g.136132755C= , CM000671.1:g.136132755C= GRCh37
NC_000009.10:g.135122576C= NCBI36
NG_006669.1:g.20300G=
NG_006669.2:g.22848G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+41G=
ENST00000647353.1:n.54-6216G=
ENST00000651471.1:n.329+674G=
ENST00000679909.1:c.28+17794G= ENSP00000506089.1:n.28+17794G=
ENST00000453660.3:n.385+41G=
ENST00000538324.2:c.371+41G= ENSP00000483018.1:n.371+41G=
ENST00000611156.4:c.371+41G= ENSP00000483265.1:n.371+41G=
NM_020469.2:c.374+41G= NP_065202.2:n.374+41G=
NM_020469.3:c.374+41G= NP_065202.2:n.374+41G=