ClinGen Allele Registry
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Canonical Allele Identifier:
CA15949664
Gene:
Linked Data
dbSNP Id:
rs266882
gnomAD v2:
19-51358013-G-A
gnomAD v3:
19-50854757-G-A
gnomAD v4:
19-50854757-G-A
MyVariant Identifiers:
chr19:g.51358013G>A (hg19)
chr19:g.50854757G>A (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.50854757G>A , CM000681.2:g.50854757G>A
GRCh38
NC_000019.9:g.51358013G>A , CM000681.1:g.51358013G>A
GRCh37
NC_000019.8:g.56049825G>A
NCBI36
NG_011653.1:g.4843G>A
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