ClinGen Allele Registry
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Canonical Allele Identifier:
CA375686401
Gene: ABO
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr9:g.136131696A>G (hg19)
chr9:g.133256309A>G (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133256309A>G , CM000671.2:g.133256309A>G
GRCh38
NC_000009.11:g.136131696A>G , CM000671.1:g.136131696A>G
GRCh37
NC_000009.10:g.135121517A>G
NCBI36
NG_006669.1:g.21359T>C
NG_006669.2:g.23907T>C
Transcript Alleles
HGVS
Amino-acid Change
ENST00000453660.4:n.451T>C
ENST00000647353.1:n.54-5157T>C
ENST00000651471.1:n.377T>C
ENST00000679909.1:c.28+18853T>C
ENSP00000506089.1:n.28+18853T>C
ENST00000453660.3:n.433T>C
ENST00000538324.2:c.419T>C
ENSP00000483018.1:p.Phe140Ser
ENST00000611156.4:c.419T>C
ENSP00000483265.1:p.Phe140Ser
NM_020469.2:c.422T>C
NP_065202.2:p.Phe141Ser
NM_020469.3:c.422T>C
NP_065202.2:p.Phe141Ser
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