Canonical Allele Identifier: CA170532287
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs948606280
gnomAD v3: 8-2649324-G-C
gnomAD v4: 8-2649324-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649324G>C , CM000670.2:g.2649324G>C GRCh38
NC_000008.10:g.2506841G>C , CM000670.1:g.2506841G>C GRCh37
NC_000008.9:g.2494248G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125425.1:n.238+25406C>G