ClinGen Allele Registry
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Canonical Allele Identifier:
CA448291343
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh37
chr6:g.205920G>C
Linked Data - NCBI & NCI
dbSNP:
5000996
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.205920G>C , CM000668.2:g.205920G>C
GRCh38
NC_000006.11:g.205920G>C , CM000668.1:g.205920G>C
GRCh37
NC_000006.10:g.150920G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'