Canonical Allele Identifier: CA100366625
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs932765279
gnomAD v2: 4-79588852-C-A
gnomAD v3: 4-78667698-C-A
gnomAD v4: 4-78667698-C-A
MyVariant Identifiers: chr4:g.79588852C>A (hg19) chr4:g.78667698C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667698C>A , CM000666.2:g.78667698C>A GRCh38
NC_000004.11:g.79588852C>A , CM000666.1:g.79588852C>A GRCh37
NC_000004.10:g.79807876C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4687C>A
NR_038304.1:n.473+4687C>A
NR_038305.1:n.380-5645C>A
NR_038306.1:n.380-13063C>A
NR_038307.1:n.364+4687C>A
NR_038308.1:n.325+4726C>A
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