Canonical Allele Identifier: CA100366630
Gene: LINC01094 HGNC NCBI

Linked Data

dbSNP Id: rs148622084
gnomAD v2: 4-79588889-G-C
gnomAD v3: 4-78667735-G-C
gnomAD v4: 4-78667735-G-C
MyVariant Identifiers: chr4:g.79588889G>C (hg19) chr4:g.78667735G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78667735G>C , CM000666.2:g.78667735G>C GRCh38
NC_000004.11:g.79588889G>C , CM000666.1:g.79588889G>C GRCh37
NC_000004.10:g.79807913G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038303.1:n.473+4724G>C
NR_038304.1:n.473+4724G>C
NR_038305.1:n.380-5608G>C
NR_038306.1:n.380-13026G>C
NR_038307.1:n.364+4724G>C
NR_038308.1:n.325+4763G>C
Search 100 bp 5'
Search 100 bp 3'