ClinGen Allele Registry
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Canonical Allele Identifier:
CA796572663
Gene:
Linked Data
dbSNP Id:
rs1291244499
MyVariant Identifiers:
chr4:g.5712769C>T (hg19)
chr4:g.5711042C>T (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.5711042C>T , CM000666.2:g.5711042C>T
GRCh38
NC_000004.11:g.5712769C>T , CM000666.1:g.5712769C>T
GRCh37
NC_000004.10:g.5763670C>T
NCBI36
NG_008843.1:g.4846C>T
NG_015821.1:g.3507G>A
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