Canonical Allele Identifier: CA850291700
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1446701574
MyVariant Identifiers: chr8:g.2506886A>C (hg19) chr8:g.2649369A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649369A>C , CM000670.2:g.2649369A>C GRCh38
NC_000008.10:g.2506886A>C , CM000670.1:g.2506886A>C GRCh37
NC_000008.9:g.2494293A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125425.1:n.238+25361T>G
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