ClinGen Allele Registry
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Canonical Allele Identifier:
CA375686469
Gene: ABO
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr9:g.136131727T>A (hg19)
chr9:g.133256340T>A (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133256340T>A , CM000671.2:g.133256340T>A
GRCh38
NC_000009.11:g.136131727T>A , CM000671.1:g.136131727T>A
GRCh37
NC_000009.10:g.135121548T>A
NCBI36
NG_006669.1:g.21328A>T
NG_006669.2:g.23876A>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000453660.4:n.420A>T
ENST00000647353.1:n.54-5188A>T
ENST00000651471.1:n.346A>T
ENST00000679909.1:c.28+18822A>T
ENSP00000506089.1:n.28+18822A>T
ENST00000453660.3:n.402A>T
ENST00000538324.2:c.388A>T
ENSP00000483018.1:p.Lys130Ter
ENST00000611156.4:c.388A>T
ENSP00000483265.1:p.Lys130Ter
NM_020469.2:c.391A>T
NP_065202.2:p.Lys131Ter
NM_020469.3:c.391A>T
NP_065202.2:p.Lys131Ter
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