Canonical Allele Identifier: CA1129725008
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274138_133274139insC , CM000671.2:g.133274138_133274139insC GRCh38
NC_000009.11:g.136149554_136149555insC , CM000671.1:g.136149554_136149555insC GRCh37
NC_000009.10:g.135139375_135139376insC NCBI36
NG_006669.1:g.3496_3497insG
NG_006669.2:g.6076_6077insG

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+1023_58+1024insG
ENST00000647353.1:n.53+1023_53+1024insG
ENST00000651471.1:n.63+1823_63+1824insG
ENST00000679909.1:c.28+1023_28+1024insG ENSP00000506089.1:n.28+1023_28+1024insG
ENST00000453660.3:n.40+1023_40+1024insG
ENST00000538324.2:c.28+1023_28+1024insG ENSP00000483018.1:n.28+1023_28+1024insG
ENST00000611156.4:c.28+1023_28+1024insG ENSP00000483265.1:n.28+1023_28+1024insG
NM_020469.2:c.28+1023_28+1024insG NP_065202.2:n.28+1023_28+1024insG
NM_020469.3:c.28+1023_28+1024insG NP_065202.2:n.28+1023_28+1024insG