Canonical Allele Identifier: CA1882582183
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257248_133257249delinsGA , CM000671.2:g.133257248_133257249delinsGA GRCh38
NC_000009.11:g.136132635_136132636delinsGA , CM000671.1:g.136132635_136132636delinsGA GRCh37
NC_000009.10:g.135122456_135122457delinsGA NCBI36
NG_006669.1:g.20419_20420delinsTC
NG_006669.2:g.22967_22968delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.403+160_403+161delinsTC
ENST00000647353.1:n.54-6097_54-6096delinsTC
ENST00000651471.1:n.329+793_329+794delinsTC
ENST00000679909.1:c.28+17913_28+17914delinsTC ENSP00000506089.1:n.28+17913_28+17914delinsTC
ENST00000453660.3:n.385+160_385+161delinsTC
ENST00000538324.2:c.371+160_371+161delinsTC ENSP00000483018.1:n.371+160_371+161delinsTC
ENST00000611156.4:c.371+160_371+161delinsTC ENSP00000483265.1:n.371+160_371+161delinsTC
NM_020469.2:c.374+160_374+161delinsTC NP_065202.2:n.374+160_374+161delinsTC
NM_020469.3:c.374+160_374+161delinsTC NP_065202.2:n.374+160_374+161delinsTC