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Canonical Allele Identifier:
CA12829723
Gene: LINC00208
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr8:g.11578007T>C
GRCh37
chr8:g.11435516T>C
Linked Data - Sequence & Population
gnomAD v2:
8:11435516 T / C
gnomAD v3:
8:11578007 T / C
gnomAD v4:
chr8-11578007-T-C
Joint Max Group AF
0.59689899 (AFR)
Genomes Max Group AF
0.59689899 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10108511
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.11578007T>C , CM000670.2:g.11578007T>C
GRCh38
NC_000008.10:g.11435516T>C , CM000670.1:g.11435516T>C
GRCh37
NC_000008.9:g.11472925T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_040035.1:n.784-363T>C
Search 100 bp 5'
Search 100 bp 3'