ClinGen Allele Registry
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Canonical Allele Identifier:
CA626470828
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.49488950G>C
GRCh37
chr17:g.47566312G>C
Linked Data - Sequence & Population
gnomAD v2:
17:47566312 G / C
gnomAD v3:
17:49488950 G / C
gnomAD v4:
chr17-49488950-G-C
Linked Data - NCBI & NCI
dbSNP:
16948200
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.49488950G>C , CM000679.2:g.49488950G>C
GRCh38
NC_000017.10:g.47566312G>C , CM000679.1:g.47566312G>C
GRCh37
NC_000017.9:g.44921311G>C
NCBI36
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