Canonical Allele Identifier: CA2692330849
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258196_133258197insA , CM000671.2:g.133258196_133258197insA GRCh38
NC_000009.11:g.136133587_136133588insA , CM000671.1:g.136133587_136133588insA GRCh37
NC_000009.10:g.135123408_135123409insA NCBI36
NG_006669.1:g.19466_19467insT
NG_006669.2:g.22018_22019insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-65_234-64insT
ENST00000647353.1:n.54-7045_54-7044insT
ENST00000651471.1:n.239-65_239-64insT
ENST00000679909.1:c.28+16965_28+16966insT ENSP00000506089.1:n.28+16965_28+16966insT
ENST00000453660.3:n.216-65_216-64insT
ENST00000538324.2:c.204-65_204-64insT ENSP00000483018.1:n.204-65_204-64insT
ENST00000611156.4:c.204-65_204-64insT ENSP00000483265.1:n.204-65_204-64insT
NM_020469.2:c.204-65_204-64insT NP_065202.2:n.204-65_204-64insT
NM_020469.3:c.204-65_204-64insT NP_065202.2:n.204-65_204-64insT