Canonical Allele Identifier: CA860756210
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1397445966
MyVariant Identifiers: chr9:g.133260301del (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260301del , CM000671.2:g.133260301del GRCh38
NC_000009.11:g.136135704del , CM000671.1:g.136135704del GRCh37
NC_000009.10:g.135125525del NCBI36
NG_006669.1:g.17349del
NG_006669.2:g.19914del

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.186-435del
ENST00000647353.1:n.54-9149del
ENST00000651471.1:n.191-435del
ENST00000679909.1:c.28+14861del ENSP00000506089.1:n.28+14861del
ENST00000453660.3:n.168-435del
ENST00000538324.2:c.156-435del ENSP00000483018.1:n.156-435del
ENST00000611156.4:c.156-435del ENSP00000483265.1:n.156-435del
NM_020469.2:c.156-435del NP_065202.2:n.156-435del
NM_020469.3:c.156-435del NP_065202.2:n.156-435del