Canonical Allele Identifier: CA1882579669
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255845_133255852delinsTGCCGTTG , CM000671.2:g.133255845_133255852delinsTGCCGTTG GRCh38
NC_000009.11:g.136131232_136131239delinsTGCCGTTG , CM000671.1:g.136131232_136131239delinsTGCCGTTG GRCh37
NC_000009.10:g.135121053_135121060delinsTGCCGTTG NCBI36
NG_006669.1:g.21816_21823delinsCAACGGCA
NG_006669.2:g.24364_24371delinsCAACGGCA

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.908_915delinsCAACGGCA
ENST00000647353.1:n.54-4700_54-4693delinsCAACGGCA
ENST00000679909.1:c.28+19310_28+19317delinsCAACGGCA ENSP00000506089.1:n.28+19310_28+19317deli...
ENST00000453660.3:n.890_897delinsCAACGGCA
ENST00000538324.2:c.876_883delinsCAACGGCA ENSP00000483018.1:p.Ala292=
ENST00000611156.4:c.876_883delinsCAACGGCA ENSP00000483265.1:p.Ala292=
NM_020469.2:c.879_886delinsCAACGGCA NP_065202.2:p.Ala293=
NM_020469.3:c.879_886delinsCAACGGCA NP_065202.2:p.Ala293=