Canonical Allele Identifier: CA170532260
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1022618283
gnomAD v3: 8-2649203-C-T
gnomAD v4: 8-2649203-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649203C>T , CM000670.2:g.2649203C>T GRCh38
NC_000008.10:g.2506720C>T , CM000670.1:g.2506720C>T GRCh37
NC_000008.9:g.2494127C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125425.1:n.238+25527G>A