ClinGen Allele Registry
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Canonical Allele Identifier:
CA154393477
Gene:
Linked Data
dbSNP Id:
rs759137387
gnomAD v3:
7-13400620-T-G
gnomAD v4:
7-13400620-T-G
MyVariant Identifiers:
chr7:g.13440245T>G (hg19)
chr7:g.13400620T>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.13400620T>G , CM000669.2:g.13400620T>G
GRCh38
NC_000007.13:g.13440245T>G , CM000669.1:g.13440245T>G
GRCh37
NC_000007.12:g.13406770T>G
NCBI36
Transcript Alleles
HGVS
Amino-acid change
XR_001745097.1:n.147+90297T>G
Search 100 bp 5'
Search 100 bp 3'