Canonical Allele Identifier: CA1882583084
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258115G= , CM000671.2:g.133258115G= GRCh38
NC_000009.11:g.136133505G= , CM000671.1:g.136133505G= GRCh37
NC_000009.10:g.135123326G= NCBI36
NG_006669.1:g.19549C=
NG_006669.2:g.22100C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.251C=
ENST00000647353.1:n.54-6963C=
ENST00000651471.1:n.256C=
ENST00000679909.1:c.28+17047C= ENSP00000506089.1:n.28+17047C=
ENST00000453660.3:n.233C=
ENST00000538324.2:c.221C= ENSP00000483018.1:p.Pro74=
ENST00000611156.4:c.221C= ENSP00000483265.1:p.Pro74=
NM_020469.2:c.221C= NP_065202.2:p.Pro74=
NM_020469.3:c.221C= NP_065202.2:p.Pro74=