ClinGen Allele Registry
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Canonical Allele Identifier:
CA817908394
Gene:
Linked Data
dbSNP Id:
rs1453324146
MyVariant Identifiers:
chr6:g.11943571C>G (hg19)
chr6:g.11943338C>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.11943338C>G , CM000668.2:g.11943338C>G
GRCh38
NC_000006.11:g.11943571C>G , CM000668.1:g.11943571C>G
GRCh37
NC_000006.10:g.12051557C>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001743976.1:n.348-8197C>G
Search 100 bp 5'
Search 100 bp 3'