ClinGen Allele Registry
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Canonical Allele Identifier:
CA112973494
Gene:
Linked Data
dbSNP Id:
rs989871798
MyVariant Identifiers:
chr5:g.1447889C>T (hg19)
chr5:g.1447774C>T (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.1447774C>T , CM000667.2:g.1447774C>T
GRCh38
NC_000005.9:g.1447889C>T , CM000667.1:g.1447889C>T
GRCh37
NC_000005.8:g.1500889C>T
NCBI36
NG_015885.1:g.2655G>A
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