ClinGen Allele Registry
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Canonical Allele Identifier:
CA841571696
Gene:
Linked Data
dbSNP Id:
rs191638893
gnomAD v3:
7-69146947-G-T
gnomAD v4:
7-69146947-G-T
MyVariant Identifiers:
chr7:g.68611934G>T (hg19)
chr7:g.69146947G>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.69146947G>T , CM000669.2:g.69146947G>T
GRCh38
NC_000007.13:g.68611934G>T , CM000669.1:g.68611934G>T
GRCh37
NC_000007.12:g.68249870G>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_927647.1:n.88-821C>A
Search 100 bp 5'
Search 100 bp 3'