ClinGen Allele Registry
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Canonical Allele Identifier:
CA186787490
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr8:g.135837811T>A
GRCh37
chr8:g.136850054T>A
Linked Data - Sequence & Population
gnomAD v2:
8:136850054 T / A
gnomAD v3:
8:135837811 T / A
gnomAD v4:
chr8-135837811-T-A
Linked Data - NCBI & NCI
dbSNP:
4385494
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.135837811T>A , CM000670.2:g.135837811T>A
GRCh38
NC_000008.10:g.136850054T>A , CM000670.1:g.136850054T>A
GRCh37
NC_000008.9:g.136919236T>A
NCBI36
Search 100 bp 5'
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