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Canonical Allele Identifier:
CA5305693
Gene: ABO
HGNC
NCBI
Linked Data
dbSNP Id:
rs782321646
ExAC:
9:136131223 C / T
gnomAD v2:
9-136131223-C-T
gnomAD v3:
9-133255836-C-T
gnomAD v4:
9-133255836-C-T
COSMIC:
COSM3375154
MyVariant Identifiers:
chr9:g.136131223C>T (hg19)
chr9:g.133255836C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133255836C>T , CM000671.2:g.133255836C>T
GRCh38
NC_000009.11:g.136131223C>T , CM000671.1:g.136131223C>T
GRCh37
NC_000009.10:g.135121044C>T
NCBI36
NG_006669.1:g.21832G>A
NG_006669.2:g.24380G>A
Transcript Alleles
HGVS
Amino-acid change
ENST00000453660.4:n.924G>A
ENST00000647353.1:n.54-4684G>A
ENST00000679909.1:c.28+19326G>A
ENSP00000506089.1:n.28+19326G>A
ENST00000453660.3:n.906G>A
ENST00000538324.2:c.892G>A
ENSP00000483018.1:p.Val298Met
ENST00000611156.4:c.892G>A
ENSP00000483265.1:p.Val298Met
NM_020469.2:c.895G>A
NP_065202.2:p.Val299Met
NM_020469.3:c.895G>A
NP_065202.2:p.Val299Met
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