Canonical Allele Identifier: CA13200998
Gene: LINC01475 HGNC NCBI
COSMIC:
COSN6475071 (not active)
MyVariant.info:
GRCh38 chr10:g.99530544T>C
GRCh37 chr10:g.101290301T>C
gnomAD v2:
10:101290301 T / C
gnomAD v3:
10:99530544 T / C
gnomAD v4:
chr10-99530544-T-C
Joint Max Group AF 0.61671072 (SAS)
Genomes Max Group AF 0.61671072 (SAS)
dbSNP:
6584283
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99530544T>C , CM000672.2:g.99530544T>C GRCh38
NC_000010.10:g.101290301T>C , CM000672.1:g.101290301T>C GRCh37
NC_000010.9:g.101280291T>C NCBI36
NG_016854.1:g.2612T>C

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.166+468A>G
Search 100 bp 5'
Search 100 bp 3'