Canonical Allele Identifier: CA860763664
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1270439547

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274099_133274115del , CM000671.2:g.133274099_133274115del GRCh38
NC_000009.11:g.136149515_136149531del , CM000671.1:g.136149515_136149531del GRCh37
NC_000009.10:g.135139336_135139352del NCBI36
NG_006669.1:g.3523_3539del
NG_006669.2:g.6103_6119del

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+1050_58+1066del
ENST00000647353.1:n.53+1050_53+1066del
ENST00000651471.1:n.63+1850_63+1866del
ENST00000679909.1:c.28+1050_28+1066del ENSP00000506089.1:n.28+1050_28+1066del
ENST00000453660.3:n.40+1050_40+1066del
ENST00000538324.2:c.28+1050_28+1066del ENSP00000483018.1:n.28+1050_28+1066del
ENST00000611156.4:c.28+1050_28+1066del ENSP00000483265.1:n.28+1050_28+1066del
NM_020469.2:c.28+1050_28+1066del NP_065202.2:n.28+1050_28+1066del
NM_020469.3:c.28+1050_28+1066del NP_065202.2:n.28+1050_28+1066del