Canonical Allele Identifier: CA918570809
Gene: ABO HGNC NCBI

Linked Data

ClinVar Variation Id: 1172910
ClinVar RCV Id: RCV001527067
dbSNP Id: rs1554760445

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274294_133274295delinsT , CM000671.2:g.133274294_133274295delinsT GRCh38
NC_000009.11:g.136149710_136149711delinsT , CM000671.1:g.136149710_136149711delinsT GRCh37
NC_000009.10:g.135139531_135139532delinsT NCBI36
NG_006669.2:g.5920_5921delinsA

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+867_58+868delinsA
ENST00000647353.1:n.53+867_53+868delinsA
ENST00000651471.1:n.63+1667_63+1668delinsA
ENST00000679909.1:c.28+867_28+868delinsA ENSP00000506089.1:n.28+867_28+868delinsA
ENST00000453660.3:n.40+867_40+868delinsA
ENST00000538324.2:c.28+867_28+868delinsA ENSP00000483018.1:n.28+867_28+868delinsA
ENST00000611156.4:c.28+867_28+868delinsA ENSP00000483265.1:n.28+867_28+868delinsA
NM_020469.2:c.28+867_28+868delinsA NP_065202.2:n.28+867_28+868delinsA
NM_020469.3:c.28+867_28+868delinsA NP_065202.2:n.28+867_28+868delinsA