Canonical Allele Identifier: CA170532291
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs906859458
gnomAD v2: 8-2506867-A-G
gnomAD v3: 8-2649350-A-G
gnomAD v4: 8-2649350-A-G
MyVariant Identifiers: chr8:g.2506867A>G (hg19) chr8:g.2649350A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649350A>G , CM000670.2:g.2649350A>G GRCh38
NC_000008.10:g.2506867A>G , CM000670.1:g.2506867A>G GRCh37
NC_000008.9:g.2494274A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125425.1:n.238+25380T>C
Search 100 bp 5'
Search 100 bp 3'