ClinGen Allele Registry
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Canonical Allele Identifier:
CA375686631
Gene: ABO
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr9:g.136132846C>G (hg19)
chr9:g.133257459C>G (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133257459C>G , CM000671.2:g.133257459C>G
GRCh38
NC_000009.11:g.136132846C>G , CM000671.1:g.136132846C>G
GRCh37
NC_000009.10:g.135122667C>G
NCBI36
NG_006669.1:g.20209G>C
NG_006669.2:g.22757G>C
Transcript Alleles
HGVS
Amino-acid Change
ENST00000453660.4:n.353G>C
ENST00000647353.1:n.54-6307G>C
ENST00000651471.1:n.329+583G>C
ENST00000679909.1:c.28+17703G>C
ENSP00000506089.1:n.28+17703G>C
ENST00000453660.3:n.335G>C
ENST00000538324.2:c.321G>C
ENSP00000483018.1:p.Gln107His
ENST00000611156.4:c.321G>C
ENSP00000483265.1:p.Gln107His
NM_020469.2:c.324G>C
NP_065202.2:p.Gln108His
NM_020469.3:c.324G>C
NP_065202.2:p.Gln108His
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