ClinGen Allele Registry
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Canonical Allele Identifier:
CA5305814
Gene: ABO
HGNC
NCBI
Linked Data
dbSNP Id:
rs56039827
ExAC:
9:136131591 C / T
gnomAD v2:
9-136131591-C-T
gnomAD v3:
9-133256204-C-T
gnomAD v4:
9-133256204-C-T
MyVariant Identifiers:
chr9:g.136131591C>T (hg19)
chr9:g.133256204C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133256204C>T , CM000671.2:g.133256204C>T
GRCh38
NC_000009.11:g.136131591C>T , CM000671.1:g.136131591C>T
GRCh37
NC_000009.10:g.135121412C>T
NCBI36
NG_006669.1:g.21464G>A
NG_006669.2:g.24012G>A
Transcript Alleles
HGVS
Amino-acid Change
ENST00000453660.4:n.556G>A
ENST00000647353.1:n.54-5052G>A
ENST00000651471.1:n.482G>A
ENST00000679909.1:c.28+18958G>A
ENSP00000506089.1:n.28+18958G>A
ENST00000453660.3:n.538G>A
ENST00000538324.2:c.524G>A
ENSP00000483018.1:p.Arg175His
ENST00000611156.4:c.524G>A
ENSP00000483265.1:p.Arg175His
NM_020469.2:c.527G>A
NP_065202.2:p.Arg176His
NM_020469.3:c.527G>A
NP_065202.2:p.Arg176His
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