Canonical Allele Identifier: CA13200987
Gene: LINC01475 HGNC NCBI

Linked Data

dbSNP Id: rs10883365
gnomAD v2: 10-101287764-G-A
gnomAD v3: 10-99528007-G-A
gnomAD v4: 10-99528007-G-A
MyVariant Identifiers: chr10:g.101287764G>A (hg19) chr10:g.99528007G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99528007G>A , CM000672.2:g.99528007G>A GRCh38
NC_000010.10:g.101287764G>A , CM000672.1:g.101287764G>A GRCh37
NC_000010.9:g.101277754G>A NCBI36
NG_016854.1:g.75G>A

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.376C>T
Search 100 bp 5'
Search 100 bp 3'