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Canonical Allele Identifier:
CA16262224
Gene: LINC02520
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.37519268T>C
GRCh37
chr6:g.37487044T>C
Linked Data - Sequence & Population
gnomAD v2:
6:37487044 T / C
gnomAD v3:
6:37519268 T / C
gnomAD v4:
chr6-37519268-T-C
Joint Max Group AF
0.6557793 (NFE)
Genomes Max Group AF
0.6557793 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1757171
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.37519268T>C , CM000668.2:g.37519268T>C
GRCh38
NC_000006.11:g.37487044T>C , CM000668.1:g.37487044T>C
GRCh37
NC_000006.10:g.37595022T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_126057.1:n.357+11564T>C
Search 100 bp 5'
Search 100 bp 3'