Canonical Allele Identifier: CA200764794
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs796317046

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255307_133255315delinsGCTGTGTGT , CM000671.2:g.133255307_133255315delinsGCTGTGTGT GRCh38
NC_000009.11:g.136130694_136130702delinsGCTGTGTGT , CM000671.1:g.136130694_136130702delinsGCTGTGTGT GRCh37
NC_000009.10:g.135120515_135120523delinsGCTGTGTGT NCBI36
NG_006669.1:g.22353_22361delinsACACACAGC
NG_006669.2:g.24901_24909delinsACACACAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1445_1453delinsACACACAGC
ENST00000647353.1:n.54-4163_54-4155delinsACACACAGC
ENST00000679909.1:c.28+19847_28+19855delinsACACACAGC ENSP00000506089.1:n.28+19847_28+19855delinsACACACAGC
ENST00000453660.3:n.1427_1435delinsACACACAGC
ENST00000611156.4:c.*351_*359delinsACACACAGC ENSP00000483265.1:n.*351_*359delinsACACACAGC
NM_020469.2:c.*351_*359delinsACACACAGC NP_065202.2:n.*351_*359delinsACACACAGC
NM_020469.3:c.*351_*359delinsACACACAGC NP_065202.2:n.*351_*359delinsACACACAGC