Canonical Allele Identifier: CA94354174
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs924702609
gnomAD v3: 4-26083948-T-C
gnomAD v4: 4-26083948-T-C
MyVariant Identifiers: chr4:g.26085570T>C (hg19) chr4:g.26083948T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083948T>C , CM000666.2:g.26083948T>C GRCh38
NC_000004.11:g.26085570T>C , CM000666.1:g.26085570T>C GRCh37
NC_000004.10:g.25694668T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3358T>C
XR_925506.3:n.1408+3358T>C
Search 100 bp 5'
Search 100 bp 3'