Canonical Allele Identifier: CA2610478028
Gene: LINC01475 HGNC NCBI

Linked Data

dbSNP Id: rs2119537628
gnomAD v4: 10-99527707-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527707C>T , CM000672.2:g.99527707C>T GRCh38
NC_000010.10:g.101287464C>T , CM000672.1:g.101287464C>T GRCh37
NC_000010.9:g.101277454C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.577+99G>A
Search 100 bp 5'
Search 100 bp 3'