ClinGen Allele Registry
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Canonical Allele Identifier:
CA476840427
Gene:
Linked Data
MyVariant Identifiers:
chr11:g.114231392A>T (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.114360670A>T , CM000673.2:g.114360670A>T
GRCh38
NC_000011.9:g.114231392A>T , CM000673.1:g.114231392A>T
GRCh37
NC_000011.8:g.113736602A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_120567.1:n.3796T>A
Search 100 bp 5'
Search 100 bp 3'