Canonical Allele Identifier: CA2692330730
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257986_133257990del , CM000671.2:g.133257986_133257990del GRCh38
NC_000009.11:g.136133373_136133377del , CM000671.1:g.136133373_136133377del GRCh37
NC_000009.10:g.135123194_135123198del NCBI36
NG_006669.1:g.19682_19686del
NG_006669.2:g.22230_22234del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.269+112_269+116del
ENST00000647353.1:n.54-6833_54-6829del
ENST00000651471.1:n.329+57_329+61del
ENST00000679909.1:c.28+17177_28+17181del ENSP00000506089.1:n.28+17177_28+17181del
ENST00000453660.3:n.251+112_251+116del
ENST00000538324.2:c.239+112_239+116del ENSP00000483018.1:n.239+112_239+116del
ENST00000611156.4:c.239+112_239+116del ENSP00000483265.1:n.239+112_239+116del
NM_020469.2:c.239+112_239+116del NP_065202.2:n.239+112_239+116del
NM_020469.3:c.239+112_239+116del NP_065202.2:n.239+112_239+116del