Canonical Allele Identifier: CA850291676
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1273071217
gnomAD v3: 8-2649311-T-G
gnomAD v4: 8-2649311-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649311T>G , CM000670.2:g.2649311T>G GRCh38
NC_000008.10:g.2506828T>G , CM000670.1:g.2506828T>G GRCh37
NC_000008.9:g.2494235T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125425.1:n.238+25419A>C