Canonical Allele Identifier: CA850291620
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1207195453
gnomAD v3: 8-2649223-G-A
gnomAD v4: 8-2649223-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649223G>A , CM000670.2:g.2649223G>A GRCh38
NC_000008.10:g.2506740G>A , CM000670.1:g.2506740G>A GRCh37
NC_000008.9:g.2494147G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125425.1:n.238+25507C>T