Canonical Allele Identifier: CA850291689
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1399429470
gnomAD v3: 8-2649345-A-T
gnomAD v4: 8-2649345-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649345A>T , CM000670.2:g.2649345A>T GRCh38
NC_000008.10:g.2506862A>T , CM000670.1:g.2506862A>T GRCh37
NC_000008.9:g.2494269A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125425.1:n.238+25385T>A