Canonical Allele Identifier: CA550489567

Gene: LINC02357

Linked Data

• dbSNP Id: rs1273294543
• gnomAD v2: 4-26085579-A-C
• gnomAD v3: 4-26083957-A-C
• gnomAD v4: 4-26083957-A-C
• MyVariant Identifiers: chr4:g.26085579A>C (hg19) ; chr4:g.26083957A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.26083957A>C , CM000666.2:g.26083957A>C	GRCh38
NC_000004.11:g.26085579A>C , CM000666.1:g.26085579A>C	GRCh37
NC_000004.10:g.25694677A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_925506.1:n.1401+3367A>C
XR_925506.3:n.1408+3367A>C