Canonical Allele Identifier: CA14458617
Gene:

Linked Data

ClinVar Variation Id: 1269387
ClinVar RCV Id: RCV001681020
dbSNP Id: rs28365859
gnomAD v2: 17-1303778-C-G
gnomAD v3: 17-1400484-C-G
gnomAD v4: 17-1400484-C-G
MyVariant Identifiers: chr17:g.1303778C>G (hg19) chr17:g.1400484C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1400484C>G , CM000679.2:g.1400484C>G GRCh38
NC_000017.10:g.1303778C>G , CM000679.1:g.1303778C>G GRCh37
NC_000017.9:g.1250528C>G NCBI36
NG_009233.1:g.4779G>C
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