Canonical Allele Identifier: CA2954282287
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257396dup , CM000671.2:g.133257396dup GRCh38
NC_000009.11:g.136132783dup , CM000671.1:g.136132783dup GRCh37
NC_000009.10:g.135122604dup NCBI36
NG_006669.1:g.20273dup
NG_006669.2:g.22821dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.403+14dup
ENST00000647353.1:n.54-6243dup
ENST00000651471.1:n.329+647dup
ENST00000679909.1:c.28+17767dup ENSP00000506089.1:n.28+17767dup
ENST00000453660.3:n.385+14dup
ENST00000538324.2:c.371+14dup ENSP00000483018.1:n.371+14dup
ENST00000611156.4:c.371+14dup ENSP00000483265.1:n.371+14dup
NM_020469.2:c.374+14dup NP_065202.2:n.374+14dup
NM_020469.3:c.374+14dup NP_065202.2:n.374+14dup