Canonical Allele Identifier: CA1129724959
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274135_133274136insCT , CM000671.2:g.133274135_133274136insCT GRCh38
NC_000009.11:g.136149551_136149552insCT , CM000671.1:g.136149551_136149552insCT GRCh37
NC_000009.10:g.135139372_135139373insCT NCBI36
NG_006669.1:g.3499_3500insAG
NG_006669.2:g.6079_6080insAG

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+1026_58+1027insAG
ENST00000647353.1:n.53+1026_53+1027insAG
ENST00000651471.1:n.63+1826_63+1827insAG
ENST00000679909.1:c.28+1026_28+1027insAG ENSP00000506089.1:n.28+1026_28+1027insAG
ENST00000453660.3:n.40+1026_40+1027insAG
ENST00000538324.2:c.28+1026_28+1027insAG ENSP00000483018.1:n.28+1026_28+1027insAG
ENST00000611156.4:c.28+1026_28+1027insAG ENSP00000483265.1:n.28+1026_28+1027insAG
NM_020469.2:c.28+1026_28+1027insAG NP_065202.2:n.28+1026_28+1027insAG
NM_020469.3:c.28+1026_28+1027insAG NP_065202.2:n.28+1026_28+1027insAG