Canonical Allele Identifier: CA2692330314
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255439_133255445del , CM000671.2:g.133255439_133255445del GRCh38
NC_000009.11:g.136130826_136130832del , CM000671.1:g.136130826_136130832del GRCh37
NC_000009.10:g.135120647_135120653del NCBI36
NG_006669.1:g.22223_22229del
NG_006669.2:g.24771_24777del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1315_1321del
ENST00000647353.1:n.54-4293_54-4287del
ENST00000679909.1:c.28+19717_28+19723del ENSP00000506089.1:n.28+19717_28+19723del
ENST00000453660.3:n.1297_1303del
ENST00000611156.4:c.*221_*227del ENSP00000483265.1:n.*221_*227del
NM_020469.2:c.*221_*227del NP_065202.2:n.*221_*227del
NM_020469.3:c.*221_*227del NP_065202.2:n.*221_*227del