Canonical Allele Identifier: CA1882582161
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257220_133257228delinsGCGAGCCCA , CM000671.2:g.133257220_133257228delinsGCGAGCCCA GRCh38
NC_000009.11:g.136132607_136132615delinsGCGAGCCCA , CM000671.1:g.136132607_136132615delinsGCGAGCCCA GRCh37
NC_000009.10:g.135122428_135122436delinsGCGAGCCCA NCBI36
NG_006669.1:g.20440_20448delinsTGGGCTCGC
NG_006669.2:g.22988_22996delinsTGGGCTCGC

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+181_403+189delinsTGGGCTCGC
ENST00000647353.1:n.54-6076_54-6068delinsTGGGCTCGC
ENST00000651471.1:n.329+814_329+822delinsTGGGCTCGC
ENST00000679909.1:c.28+17934_28+17942delinsTGGGCTCGC ENSP00000506089.1:n.28+17934_28+17942deli...
ENST00000453660.3:n.385+181_385+189delinsTGGGCTCGC
ENST00000538324.2:c.371+181_371+189delinsTGGGCTCGC ENSP00000483018.1:n.371+181_371+189delins...
ENST00000611156.4:c.371+181_371+189delinsTGGGCTCGC ENSP00000483265.1:n.371+181_371+189delins...
NM_020469.2:c.374+181_374+189delinsTGGGCTCGC NP_065202.2:n.374+181_374+189delinsTGGGCT...
NM_020469.3:c.374+181_374+189delinsTGGGCTCGC NP_065202.2:n.374+181_374+189delinsTGGGCT...