ClinGen Allele Registry
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Canonical Allele Identifier:
CA631018502
Gene:
Linked Data
dbSNP Id:
rs1285789802
gnomAD v2:
19-1103731-C-T
gnomAD v3:
19-1103732-C-T
gnomAD v4:
19-1103732-C-T
MyVariant Identifiers:
chr19:g.1103731C>T (hg19)
chr19:g.1103732C>T (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.1103732C>T , CM000681.2:g.1103732C>T
GRCh38
NC_000019.9:g.1103731C>T , CM000681.1:g.1103731C>T
GRCh37
NC_000019.8:g.1054731C>T
NCBI36
NG_050621.1:g.4807C>T
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