ClinGen Allele Registry
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Canonical Allele Identifier:
CA12805588
Gene: FAM167A-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs2002030
gnomAD v2:
8-11276542-T-C
gnomAD v3:
8-11419033-T-C
gnomAD v4:
8-11419033-T-C
MyVariant Identifiers:
chr8:g.11276542T>C (hg19)
chr8:g.11419033T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.11419033T>C , CM000670.2:g.11419033T>C
GRCh38
NC_000008.10:g.11276542T>C , CM000670.1:g.11276542T>C
GRCh37
NC_000008.9:g.11313952T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_026814.1:n.341-14887T>C
Search 100 bp 5'
Search 100 bp 3'