ClinGen Allele Registry
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Canonical Allele Identifier:
CA680374188
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.76600576G>T
GRCh37
chr11:g.76311620G>T
Linked Data - Sequence & Population
gnomAD v3:
11:76600576 G / T
gnomAD v4:
chr11-76600576-G-T
Linked Data - NCBI & NCI
dbSNP:
7124842
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.76600576G>T , CM000673.2:g.76600576G>T
GRCh38
NC_000011.9:g.76311620G>T , CM000673.1:g.76311620G>T
GRCh37
NC_000011.8:g.75989268G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'