ClinGen Allele Registry
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Canonical Allele Identifier:
CA783226100
Gene:
Linked Data
dbSNP Id:
rs1174479418
MyVariant Identifiers:
chr19:g.1107012T>C (hg19)
chr19:g.1107013T>C (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.1107013T>C , CM000681.2:g.1107013T>C
GRCh38
NC_000019.9:g.1107012T>C , CM000681.1:g.1107012T>C
GRCh37
NC_000019.8:g.1058012T>C
NCBI36
NG_050621.1:g.8088T>C
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