Canonical Allele Identifier: CA2692330306
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255390_133255459del , CM000671.2:g.133255390_133255459del GRCh38
NC_000009.11:g.136130777_136130846del , CM000671.1:g.136130777_136130846del GRCh37
NC_000009.10:g.135120598_135120667del NCBI36
NG_006669.1:g.22210_22279del
NG_006669.2:g.24758_24827del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1302_1371del
ENST00000647353.1:n.54-4306_54-4237del
ENST00000679909.1:c.28+19704_28+19773del ENSP00000506089.1:n.28+19704_28+19773del
ENST00000453660.3:n.1284_1353del
ENST00000611156.4:c.*208_*277del ENSP00000483265.1:n.*208_*277del
NM_020469.2:c.*208_*277del NP_065202.2:n.*208_*277del
NM_020469.3:c.*208_*277del NP_065202.2:n.*208_*277del