Canonical Allele Identifier: CA948444187
Gene: LINC01465 HGNC NCBI

Linked Data

dbSNP Id: rs2075631038
gnomAD v3: 12-62603406-G-A
gnomAD v4: 12-62603406-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.62603406G>A , CM000674.2:g.62603406G>A GRCh38
NC_000012.11:g.62997186G>A , CM000674.1:g.62997186G>A GRCh37
NC_000012.10:g.61283453G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121682.1:n.29C>T
Search 100 bp 5'
Search 100 bp 3'