Canonical Allele Identifier: CA579528857
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1393451997
gnomAD v2: 8-2506680-A-G
gnomAD v3: 8-2649163-A-G
gnomAD v4: 8-2649163-A-G
MyVariant Identifiers: chr8:g.2506680A>G (hg19) chr8:g.2649163A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649163A>G , CM000670.2:g.2649163A>G GRCh38
NC_000008.10:g.2506680A>G , CM000670.1:g.2506680A>G GRCh37
NC_000008.9:g.2494087A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25567T>C
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