Canonical Allele Identifier: CA94354157
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs997236107
gnomAD v3: 4-26083849-T-C
gnomAD v4: 4-26083849-T-C
MyVariant Identifiers: chr4:g.26085471T>C (hg19) chr4:g.26083849T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083849T>C , CM000666.2:g.26083849T>C GRCh38
NC_000004.11:g.26085471T>C , CM000666.1:g.26085471T>C GRCh37
NC_000004.10:g.25694569T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3259T>C
XR_925506.3:n.1408+3259T>C
Search 100 bp 5'
Search 100 bp 3'