Canonical Allele Identifier: CA1882582766
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257790_133257792delinsGGC , CM000671.2:g.133257790_133257792delinsGGC GRCh38
NC_000009.11:g.136133177_136133179delinsGGC , CM000671.1:g.136133177_136133179delinsGGC GRCh37
NC_000009.10:g.135122998_135123000delinsGGC NCBI36
NG_006669.1:g.19875_19877delinsGCC
NG_006669.2:g.22423_22425delinsGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-250_270-248delinsGCC
ENST00000647353.1:n.54-6640_54-6638delinsGCC
ENST00000651471.1:n.329+250_329+252delinsGCC
ENST00000679909.1:c.28+17370_28+17372delinsGCC ENSP00000506089.1:n.28+17370_28+17372delinsGCC
ENST00000453660.3:n.252-250_252-248delinsGCC
ENST00000538324.2:c.240-250_240-248delinsGCC ENSP00000483018.1:n.240-250_240-248delinsGCC
ENST00000611156.4:c.240-250_240-248delinsGCC ENSP00000483265.1:n.240-250_240-248delinsGCC
NM_020469.2:c.240-250_240-248delinsGCC NP_065202.2:n.240-250_240-248delinsGCC
NM_020469.3:c.240-250_240-248delinsGCC NP_065202.2:n.240-250_240-248delinsGCC