Canonical Allele Identifier: CA16189751
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs115882734
gnomAD v2: 4-79589063-G-C
gnomAD v3: 4-78667909-G-C
gnomAD v4: 4-78667909-G-C
MyVariant Identifiers: chr4:g.79589063G>C (hg19) chr4:g.78667909G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667909G>C , CM000666.2:g.78667909G>C GRCh38
NC_000004.11:g.79589063G>C , CM000666.1:g.79589063G>C GRCh37
NC_000004.10:g.79808087G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4898G>C
NR_038304.1:n.473+4898G>C
NR_038305.1:n.380-5434G>C
NR_038306.1:n.380-12852G>C
NR_038307.1:n.364+4898G>C
NR_038308.1:n.325+4937G>C
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