Canonical Allele Identifier: CA931728163
Gene: LINC01475 HGNC NCBI

Linked Data

dbSNP Id: rs2033871096
gnomAD v3: 10-99527793-T-C
gnomAD v4: 10-99527793-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527793T>C , CM000672.2:g.99527793T>C GRCh38
NC_000010.10:g.101287550T>C , CM000672.1:g.101287550T>C GRCh37
NC_000010.9:g.101277540T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.577+13A>G
Search 100 bp 5'
Search 100 bp 3'