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Canonical Allele Identifier:
CA15829331
Gene: LINC01551
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr14:g.28780143T>G
GRCh37
chr14:g.29249349T>G
Linked Data - Sequence & Population
gnomAD v2:
14:29249349 T / G
gnomAD v3:
14:28780143 T / G
gnomAD v4:
chr14-28780143-T-G
Joint Max Group AF
0.27780444 (AMR)
Genomes Max Group AF
0.27780444 (AMR)
Linked Data - NCBI & NCI
dbSNP:
2038256
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.28780143T>G , CM000676.2:g.28780143T>G
GRCh38
NC_000014.8:g.29249349T>G , CM000676.1:g.29249349T>G
GRCh37
NC_000014.7:g.28319100T>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_026731.1:n.226+6710T>G
Search 100 bp 5'
Search 100 bp 3'