Canonical Allele Identifier: CA156202029
Gene: LINC02981 HGNC NCBI

Linked Data

dbSNP Id: rs556153816
gnomAD v3: 7-26442325-C-A
gnomAD v4: 7-26442325-C-A
MyVariant Identifiers: chr7:g.26481945C>A (hg19) chr7:g.26442325C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26442325C>A , CM000669.2:g.26442325C>A GRCh38
NC_000007.13:g.26481945C>A , CM000669.1:g.26481945C>A GRCh37
NC_000007.12:g.26448470C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011515671.1:c.336-18041C>A XP_011513973.1:n.336-18041C>A
NR_148499.1:n.630+30086C>A
NR_148500.1:n.225+30086C>A
NR_148501.1:n.508+30086C>A
NR_148502.1:n.453+43304C>A
NR_148503.1:n.630+30086C>A
NR_148504.1:n.630+30086C>A
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