Canonical Allele Identifier: CA550489536

Gene: LINC02357

Linked Data

• dbSNP Id: rs1393816459
• gnomAD v2: 4-26085461-A-C
• gnomAD v3: 4-26083839-A-C
• gnomAD v4: 4-26083839-A-C
• MyVariant Identifiers: chr4:g.26085461A>C (hg19) ; chr4:g.26083839A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.26083839A>C , CM000666.2:g.26083839A>C	GRCh38
NC_000004.11:g.26085461A>C , CM000666.1:g.26085461A>C	GRCh37
NC_000004.10:g.25694559A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_925506.1:n.1401+3249A>C
XR_925506.3:n.1408+3249A>C