ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA833583501
Gene:
Linked Data
dbSNP Id:
rs1215604082
gnomAD v3:
7-13400675-T-C
gnomAD v4:
7-13400675-T-C
MyVariant Identifiers:
chr7:g.13440300T>C (hg19)
chr7:g.13400675T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.13400675T>C , CM000669.2:g.13400675T>C
GRCh38
NC_000007.13:g.13440300T>C , CM000669.1:g.13440300T>C
GRCh37
NC_000007.12:g.13406825T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001745097.1:n.147+90352T>C
Search 100 bp 5'
Search 100 bp 3'