Canonical Allele Identifier: CA200765954
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs377152560

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257220_133257221insTGAGCCCA , CM000671.2:g.133257220_133257221insTGAGCCCA GRCh38
NC_000009.11:g.136132607_136132608insTGAGCCCA , CM000671.1:g.136132607_136132608insTGAGCCCA GRCh37
NC_000009.10:g.135122428_135122429insTGAGCCCA NCBI36
NG_006669.1:g.20447_20448insTGGGCTCA
NG_006669.2:g.22995_22996insTGGGCTCA

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+188_403+189insTGGGCTCA
ENST00000647353.1:n.54-6069_54-6068insTGGGCTCA
ENST00000651471.1:n.329+821_329+822insTGGGCTCA
ENST00000679909.1:c.28+17941_28+17942insTGGGCTCA ENSP00000506089.1:n.28+17941_28+17942insT...
ENST00000453660.3:n.385+188_385+189insTGGGCTCA
ENST00000538324.2:c.371+188_371+189insTGGGCTCA ENSP00000483018.1:n.371+188_371+189insTGG...
ENST00000611156.4:c.371+188_371+189insTGGGCTCA ENSP00000483265.1:n.371+188_371+189insTGG...
NM_020469.2:c.374+188_374+189insTGGGCTCA NP_065202.2:n.374+188_374+189insTGGGCTCA
NM_020469.3:c.374+188_374+189insTGGGCTCA NP_065202.2:n.374+188_374+189insTGGGCTCA