Canonical Allele Identifier: CA170532283
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs116035208
gnomAD v2: 8-2506825-C-T
gnomAD v3: 8-2649308-C-T
gnomAD v4: 8-2649308-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649308C>T , CM000670.2:g.2649308C>T GRCh38
NC_000008.10:g.2506825C>T , CM000670.1:g.2506825C>T GRCh37
NC_000008.9:g.2494232C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125425.1:n.238+25422G>A