Canonical Allele Identifier: CA2741060185
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258003_133258009del , CM000671.2:g.133258003_133258009del GRCh38
NC_000009.11:g.136133393_136133399del , CM000671.1:g.136133393_136133399del GRCh37
NC_000009.10:g.135123214_135123220del NCBI36
NG_006669.1:g.19655_19661del
NG_006669.2:g.22206_22212del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.269+88_269+94del
ENST00000647353.1:n.54-6857_54-6851del
ENST00000651471.1:n.329+33_329+39del
ENST00000679909.1:c.28+17153_28+17159del ENSP00000506089.1:n.28+17153_28+17159del
ENST00000453660.3:n.251+88_251+94del
ENST00000538324.2:c.239+88_239+94del ENSP00000483018.1:n.239+88_239+94del
ENST00000611156.4:c.239+88_239+94del ENSP00000483265.1:n.239+88_239+94del
NM_020469.2:c.239+88_239+94del NP_065202.2:n.239+88_239+94del
NM_020469.3:c.239+88_239+94del NP_065202.2:n.239+88_239+94del