Canonical Allele Identifier: CA1882579996
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255957_133255964delinsCTTGGGGA , CM000671.2:g.133255957_133255964delinsCTTGGGGA GRCh38
NC_000009.11:g.136131344_136131351delinsCTTGGGGA , CM000671.1:g.136131344_136131351delinsCTTGGGGA GRCh37
NC_000009.10:g.135121165_135121172delinsCTTGGGGA NCBI36
NG_006669.1:g.21704_21711delinsTCCCCAAG
NG_006669.2:g.24252_24259delinsTCCCCAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.796_803delinsTCCCCAAG
ENST00000647353.1:n.54-4812_54-4805delinsTCCCCAAG
ENST00000679909.1:c.28+19198_28+19205delinsTCCCCAAG ENSP00000506089.1:n.28+19198_28+19205deli...
ENST00000453660.3:n.778_785delinsTCCCCAAG
ENST00000538324.2:c.764_771delinsTCCCCAAG ENSP00000483018.1:p.Ile255=
ENST00000611156.4:c.764_771delinsTCCCCAAG ENSP00000483265.1:p.Ile255=
NM_020469.2:c.767_774delinsTCCCCAAG NP_065202.2:p.Ile256=
NM_020469.3:c.767_774delinsTCCCCAAG NP_065202.2:p.Ile256=