ClinGen Allele Registry
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Canonical Allele Identifier:
CA134173703
Gene:
Linked Data
dbSNP Id:
rs914059970
MyVariant Identifiers:
chr6:g.11943670G>A (hg19)
chr6:g.11943437G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.11943437G>A , CM000668.2:g.11943437G>A
GRCh38
NC_000006.11:g.11943670G>A , CM000668.1:g.11943670G>A
GRCh37
NC_000006.10:g.12051656G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001743976.1:n.348-8098G>A
Search 100 bp 5'
Search 100 bp 3'