Canonical Allele Identifier: CA792439282
Gene: LINC02515 HGNC NCBI

Linked Data

dbSNP Id: rs1269974328
gnomAD v3: 4-187424163-A-T
gnomAD v4: 4-187424163-A-T
MyVariant Identifiers: chr4:g.188345317A>T (hg19) chr4:g.187424163A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.187424163A>T , CM000666.2:g.187424163A>T GRCh38
NC_000004.11:g.188345317A>T , CM000666.1:g.188345317A>T GRCh37
NC_000004.10:g.188582311A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038931.1:n.322+81129T>A
XR_939603.1:n.268+1166A>T
XR_001741954.1:n.258+10452A>T
XR_001741955.1:n.1517+1166A>T
XR_001741956.1:n.258+10452A>T
XR_939603.2:n.269+1166A>T
Search 100 bp 5'
Search 100 bp 3'