ClinGen Allele Registry
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Canonical Allele Identifier:
CA12262309
Gene:
Linked Data
dbSNP Id:
rs1205864
gnomAD v2:
6-11943595-A-G
gnomAD v3:
6-11943362-A-G
gnomAD v4:
6-11943362-A-G
MyVariant Identifiers:
chr6:g.11943595A>G (hg19)
chr6:g.11943362A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.11943362A>G , CM000668.2:g.11943362A>G
GRCh38
NC_000006.11:g.11943595A>G , CM000668.1:g.11943595A>G
GRCh37
NC_000006.10:g.12051581A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001743976.1:n.348-8173A>G
Search 100 bp 5'
Search 100 bp 3'