ClinGen Allele Registry
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Canonical Allele Identifier:
CA702501656
Gene:
Linked Data
dbSNP Id:
rs1235731481
gnomAD v3:
13-94853053-C-T
gnomAD v4:
13-94853053-C-T
MyVariant Identifiers:
chr13:g.95505307C>T (hg19)
chr13:g.94853053C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.94853053C>T , CM000675.2:g.94853053C>T
GRCh38
NC_000013.10:g.95505307C>T , CM000675.1:g.95505307C>T
GRCh37
NC_000013.9:g.94303308C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_110754.1:n.257-52411C>T
Search 100 bp 5'
Search 100 bp 3'