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Canonical Allele Identifier:
CA15411590
Gene: LINC01470
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.152908893T>G
GRCh37
chr5:g.152288453T>G
Linked Data - Sequence & Population
gnomAD v2:
5:152288453 T / G
gnomAD v3:
5:152908893 T / G
gnomAD v4:
chr5-152908893-T-G
Joint Max Group AF
0.91066104 (EAS)
Genomes Max Group AF
0.91066104 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4262150
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.152908893T>G , CM000667.2:g.152908893T>G
GRCh38
NC_000005.9:g.152288453T>G , CM000667.1:g.152288453T>G
GRCh37
NC_000005.8:g.152268646T>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_109877.1:n.178+57348A>C
Search 100 bp 5'
Search 100 bp 3'