ClinGen Allele Registry
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Canonical Allele Identifier:
CA473651168
Gene:
Linked Data
MyVariant Identifiers:
chr11:g.27505651A>T (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.27484104A>T , CM000673.2:g.27484104A>T
GRCh38
NC_000011.9:g.27505651A>T , CM000673.1:g.27505651A>T
GRCh37
NC_000011.8:g.27462227A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000496450.1:n.255A>T
Search 100 bp 5'
Search 100 bp 3'