Canonical Allele Identifier: CA1882582919
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257980_133257982delinsTGA , CM000671.2:g.133257980_133257982delinsTGA GRCh38
NC_000009.11:g.136133367_136133369delinsTGA , CM000671.1:g.136133367_136133369delinsTGA GRCh37
NC_000009.10:g.135123188_135123190delinsTGA NCBI36
NG_006669.1:g.19685_19687delinsTCA
NG_006669.2:g.22233_22235delinsTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.269+115_269+117delinsTCA
ENST00000647353.1:n.54-6830_54-6828delinsTCA
ENST00000651471.1:n.329+60_329+62delinsTCA
ENST00000679909.1:c.28+17180_28+17182delinsTCA ENSP00000506089.1:n.28+17180_28+17182delinsTCA
ENST00000453660.3:n.251+115_251+117delinsTCA
ENST00000538324.2:c.239+115_239+117delinsTCA ENSP00000483018.1:n.239+115_239+117delinsTCA
ENST00000611156.4:c.239+115_239+117delinsTCA ENSP00000483265.1:n.239+115_239+117delinsTCA
NM_020469.2:c.239+115_239+117delinsTCA NP_065202.2:n.239+115_239+117delinsTCA
NM_020469.3:c.239+115_239+117delinsTCA NP_065202.2:n.239+115_239+117delinsTCA