Canonical Allele Identifier: CA200765958
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs8176724

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257238_133257245del , CM000671.2:g.133257238_133257245del GRCh38
NC_000009.11:g.136132625_136132632del , CM000671.1:g.136132625_136132632del GRCh37
NC_000009.10:g.135122446_135122453del NCBI36
NG_006669.1:g.20440_20447del

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+181_403+188del
ENST00000647353.1:n.54-6076_54-6069del
ENST00000651471.1:n.329+814_329+821del
ENST00000679909.1:c.28+17934_28+17941del ENSP00000506089.1:n.28+17934_28+17941del
ENST00000453660.3:n.385+181_385+188del
ENST00000538324.2:c.371+181_371+188del ENSP00000483018.1:n.371+181_371+188del
ENST00000611156.4:c.371+181_371+188del ENSP00000483265.1:n.371+181_371+188del
NM_020469.2:c.374+181_374+188del NP_065202.2:n.374+181_374+188del
NM_020469.3:c.374+181_374+188del NP_065202.2:n.374+181_374+188del