Canonical Allele Identifier: CA1129724758
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274122_133274128del , CM000671.2:g.133274122_133274128del GRCh38
NC_000009.11:g.136149538_136149544del , CM000671.1:g.136149538_136149544del GRCh37
NC_000009.10:g.135139359_135139365del NCBI36
NG_006669.1:g.3507_3513del
NG_006669.2:g.6087_6093del

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+1034_58+1040del
ENST00000647353.1:n.53+1034_53+1040del
ENST00000651471.1:n.63+1834_63+1840del
ENST00000679909.1:c.28+1034_28+1040del ENSP00000506089.1:n.28+1034_28+1040del
ENST00000453660.3:n.40+1034_40+1040del
ENST00000538324.2:c.28+1034_28+1040del ENSP00000483018.1:n.28+1034_28+1040del
ENST00000611156.4:c.28+1034_28+1040del ENSP00000483265.1:n.28+1034_28+1040del
NM_020469.2:c.28+1034_28+1040del NP_065202.2:n.28+1034_28+1040del
NM_020469.3:c.28+1034_28+1040del NP_065202.2:n.28+1034_28+1040del