ClinGen Allele Registry
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Canonical Allele Identifier:
CA5305788
Gene: ABO
HGNC
NCBI
Linked Data
dbSNP Id:
rs782457135
ExAC:
9:136131492 C / A
gnomAD v2:
9-136131492-C-A
gnomAD v4:
9-133256105-C-A
MyVariant Identifiers:
chr9:g.136131492C>A (hg19)
chr9:g.133256105C>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133256105C>A , CM000671.2:g.133256105C>A
GRCh38
NC_000009.11:g.136131492C>A , CM000671.1:g.136131492C>A
GRCh37
NC_000009.10:g.135121313C>A
NCBI36
NG_006669.1:g.21563G>T
NG_006669.2:g.24111G>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000453660.4:n.655G>T
ENST00000647353.1:n.54-4953G>T
ENST00000679909.1:c.28+19057G>T
ENSP00000506089.1:n.28+19057G>T
ENST00000453660.3:n.637G>T
ENST00000538324.2:c.623G>T
ENSP00000483018.1:p.Cys208Phe
ENST00000611156.4:c.623G>T
ENSP00000483265.1:p.Cys208Phe
NM_020469.2:c.626G>T
NP_065202.2:p.Cys209Phe
NM_020469.3:c.626G>T
NP_065202.2:p.Cys209Phe
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