Canonical Allele Identifier: CA2692330752
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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