ClinGen Allele Registry
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Canonical Allele Identifier:
CA736160755
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.45329012T>C
GRCh37
chr1:g.45794684T>C
Linked Data - NCBI & NCI
dbSNP:
1208877698
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.45329012T>C , CM000663.2:g.45329012T>C
GRCh38
NC_000001.10:g.45794684T>C , CM000663.1:g.45794684T>C
GRCh37
NC_000001.9:g.45567271T>C
NCBI36
NG_008189.1:g.16459A>G , LRG_220:g.16459A>G
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