Canonical Allele Identifier: CA1882582181
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257245_133257247delinsCAT , CM000671.2:g.133257245_133257247delinsCAT GRCh38
NC_000009.11:g.136132632_136132634delinsCAT , CM000671.1:g.136132632_136132634delinsCAT GRCh37
NC_000009.10:g.135122453_135122455delinsCAT NCBI36
NG_006669.1:g.20421_20423delinsATG

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+162_403+164delinsATG
ENST00000647353.1:n.54-6095_54-6093delinsATG
ENST00000651471.1:n.329+795_329+797delinsATG
ENST00000679909.1:c.28+17915_28+17917delinsATG ENSP00000506089.1:n.28+17915_28+17917deli...
ENST00000453660.3:n.385+162_385+164delinsATG
ENST00000538324.2:c.371+162_371+164delinsATG ENSP00000483018.1:n.371+162_371+164delins...
ENST00000611156.4:c.371+162_371+164delinsATG ENSP00000483265.1:n.371+162_371+164delins...
NM_020469.2:c.374+162_374+164delinsATG NP_065202.2:n.374+162_374+164delinsATG
NM_020469.3:c.374+162_374+164delinsATG NP_065202.2:n.374+162_374+164delinsATG