Canonical Allele Identifier: CA1882581024
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256367G= , CM000671.2:g.133256367G= GRCh38
NC_000009.11:g.136131754G= , CM000671.1:g.136131754G= GRCh37
NC_000009.10:g.135121575G= NCBI36
NG_006669.1:g.21301C=
NG_006669.2:g.23849C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.404-11C=
ENST00000647353.1:n.54-5215C=
ENST00000651471.1:n.330-11C=
ENST00000679909.1:c.28+18795C= ENSP00000506089.1:n.28+18795C=
ENST00000453660.3:n.386-11C=
ENST00000538324.2:c.372-11C= ENSP00000483018.1:n.372-11C=
ENST00000611156.4:c.372-11C= ENSP00000483265.1:n.372-11C=
NM_020469.2:c.375-11C= NP_065202.2:n.375-11C=
NM_020469.3:c.375-11C= NP_065202.2:n.375-11C=