Canonical Allele Identifier: CA1129725002
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274137_133274138insC , CM000671.2:g.133274137_133274138insC GRCh38
NC_000009.11:g.136149553_136149554insC , CM000671.1:g.136149553_136149554insC GRCh37
NC_000009.10:g.135139374_135139375insC NCBI36
NG_006669.1:g.3497_3498insG
NG_006669.2:g.6077_6078insG

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+1024_58+1025insG
ENST00000647353.1:n.53+1024_53+1025insG
ENST00000651471.1:n.63+1824_63+1825insG
ENST00000679909.1:c.28+1024_28+1025insG ENSP00000506089.1:n.28+1024_28+1025insG
ENST00000453660.3:n.40+1024_40+1025insG
ENST00000538324.2:c.28+1024_28+1025insG ENSP00000483018.1:n.28+1024_28+1025insG
ENST00000611156.4:c.28+1024_28+1025insG ENSP00000483265.1:n.28+1024_28+1025insG
NM_020469.2:c.28+1024_28+1025insG NP_065202.2:n.28+1024_28+1025insG
NM_020469.3:c.28+1024_28+1025insG NP_065202.2:n.28+1024_28+1025insG