ClinGen Allele Registry
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Canonical Allele Identifier:
CA12501163
Gene:
Linked Data
dbSNP Id:
rs12700667
gnomAD v2:
7-25901639-G-A
gnomAD v3:
7-25862019-G-A
gnomAD v4:
7-25862019-G-A
MyVariant Identifiers:
chr7:g.25901639G>A (hg19)
chr7:g.25862019G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.25862019G>A , CM000669.2:g.25862019G>A
GRCh38
NC_000007.13:g.25901639G>A , CM000669.1:g.25901639G>A
GRCh37
NC_000007.12:g.25868164G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
XR_927109.1:n.122+125C>T
Search 100 bp 5'
Search 100 bp 3'