Canonical Allele Identifier: CA16093999
Gene: LINC01317 HGNC NCBI

Linked Data

dbSNP Id: rs13407683
gnomAD v2: 2-34477438-G-A
gnomAD v3: 2-34252371-G-A
gnomAD v4: 2-34252371-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.34252371G>A , CM000664.2:g.34252371G>A GRCh38
NC_000002.11:g.34477438G>A , CM000664.1:g.34477438G>A GRCh37
NC_000002.10:g.34330942G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_126403.1:n.390-34272G>A