ClinGen Allele Registry
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Canonical Allele Identifier:
CA675884880
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr11:g.35071523A>T
GRCh37
chr11:g.35093070A>T
Linked Data - NCBI & NCI
dbSNP:
2785197
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.35071523A>T , CM000673.2:g.35071523A>T
GRCh38
NC_000011.9:g.35093070A>T , CM000673.1:g.35093070A>T
GRCh37
NC_000011.8:g.35049646A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001748182.1:n.41+2394T>A
Search 100 bp 5'
Search 100 bp 3'