Canonical Allele Identifier: CA156202012
Gene: LINC02981 HGNC NCBI

Linked Data

dbSNP Id: rs900337608
gnomAD v2: 7-26481875-T-C
gnomAD v3: 7-26442255-T-C
gnomAD v4: 7-26442255-T-C
MyVariant Identifiers: chr7:g.26481875T>C (hg19) chr7:g.26442255T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26442255T>C , CM000669.2:g.26442255T>C GRCh38
NC_000007.13:g.26481875T>C , CM000669.1:g.26481875T>C GRCh37
NC_000007.12:g.26448400T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011515671.1:c.336-18111T>C XP_011513973.1:n.336-18111T>C
NR_148499.1:n.630+30016T>C
NR_148500.1:n.225+30016T>C
NR_148501.1:n.508+30016T>C
NR_148502.1:n.453+43234T>C
NR_148503.1:n.630+30016T>C
NR_148504.1:n.630+30016T>C
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