ClinGen Allele Registry
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Canonical Allele Identifier:
CA553112494
Gene:
Linked Data
dbSNP Id:
rs1364113868
gnomAD v2:
4-100395432-T-C
gnomAD v3:
4-99474275-T-C
gnomAD v4:
4-99474275-T-C
MyVariant Identifiers:
chr4:g.100395432T>C (hg19)
chr4:g.99474275T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.99474275T>C , CM000666.2:g.99474275T>C
GRCh38
NC_000004.11:g.100395432T>C , CM000666.1:g.100395432T>C
GRCh37
NC_000004.10:g.100614455T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000506494.1:n.243-2413A>G
Search 100 bp 5'
Search 100 bp 3'