ClinGen Allele Registry
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Canonical Allele Identifier:
CA100084165
Gene:
Linked Data
dbSNP Id:
rs1028815467
MyVariant Identifiers:
chr4:g.74554181C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.74554181C>T , CM000666.2:g.74554181C>T
GRCh38
NC_000004.11:g.75419898C>T , CM000666.1:g.75419898C>T
GRCh37
NC_000004.10:g.75638762C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001741513.1:n.167-1349G>A
Search 100 bp 5'
Search 100 bp 3'