ClinGen Allele Registry
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Canonical Allele Identifier:
CA375682264
Gene: ABO
HGNC
NCBI
Linked Data
dbSNP Id:
rs1488664033
gnomAD v2:
9-136131038-G-A
gnomAD v3:
9-133255651-G-A
gnomAD v4:
9-133255651-G-A
MyVariant Identifiers:
chr9:g.136131038G>A (hg19)
chr9:g.133255651G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133255651G>A , CM000671.2:g.133255651G>A
GRCh38
NC_000009.11:g.136131038G>A , CM000671.1:g.136131038G>A
GRCh37
NC_000009.10:g.135120859G>A
NCBI36
NG_006669.1:g.22017C>T
NG_006669.2:g.24565C>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000453660.4:n.1109C>T
ENST00000647353.1:n.54-4499C>T
ENST00000679909.1:c.28+19511C>T
ENSP00000506089.1:n.28+19511C>T
ENST00000453660.3:n.1091C>T
ENST00000538324.2:c.1073C>T
ENSP00000483018.1:p.Ala358Val
ENST00000611156.4:c.*15C>T
ENSP00000483265.1:n.*15C>T
NM_020469.2:c.*15C>T
NP_065202.2:n.*15C>T
NM_020469.3:c.*15C>T
NP_065202.2:n.*15C>T
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