Canonical Allele Identifier: CA1882583005
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258074_133258076delinsTCA , CM000671.2:g.133258074_133258076delinsTCA GRCh38
NC_000009.11:g.136133464_136133466delinsTCA , CM000671.1:g.136133464_136133466delinsTCA GRCh37
NC_000009.10:g.135123285_135123287delinsTCA NCBI36
NG_006669.1:g.19588_19590delinsTGA
NG_006669.2:g.22139_22141delinsTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.269+21_269+23delinsTGA
ENST00000647353.1:n.54-6924_54-6922delinsTGA
ENST00000651471.1:n.295_297delinsTGA
ENST00000679909.1:c.28+17086_28+17088delinsTGA ENSP00000506089.1:n.28+17086_28+17088delinsTGA
ENST00000453660.3:n.251+21_251+23delinsTGA
ENST00000538324.2:c.239+21_239+23delinsTGA ENSP00000483018.1:n.239+21_239+23delinsTGA
ENST00000611156.4:c.239+21_239+23delinsTGA ENSP00000483265.1:n.239+21_239+23delinsTGA
NM_020469.2:c.239+21_239+23delinsTGA NP_065202.2:n.239+21_239+23delinsTGA
NM_020469.3:c.239+21_239+23delinsTGA NP_065202.2:n.239+21_239+23delinsTGA