Canonical Allele Identifier: CA2579497390
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258011_133258012del , CM000671.2:g.133258011_133258012del GRCh38
NC_000009.11:g.136133401_136133402del , CM000671.1:g.136133401_136133402del GRCh37
NC_000009.10:g.135123222_135123223del NCBI36
NG_006669.1:g.19654_19655del
NG_006669.2:g.22205_22206del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.269+87_269+88del
ENST00000647353.1:n.54-6858_54-6857del
ENST00000651471.1:n.329+32_329+33del
ENST00000679909.1:c.28+17152_28+17153del ENSP00000506089.1:n.28+17152_28+17153del
ENST00000453660.3:n.251+87_251+88del
ENST00000538324.2:c.239+87_239+88del ENSP00000483018.1:n.239+87_239+88del
ENST00000611156.4:c.239+87_239+88del ENSP00000483265.1:n.239+87_239+88del
NM_020469.2:c.239+87_239+88del NP_065202.2:n.239+87_239+88del
NM_020469.3:c.239+87_239+88del NP_065202.2:n.239+87_239+88del