Canonical Allele Identifier: CA112636665

Gene: LINC02515

Linked Data

• dbSNP Id: rs115175930
• gnomAD v2: 4-188345333-G-C
• gnomAD v3: 4-187424179-G-C
• gnomAD v4: 4-187424179-G-C
• MyVariant Identifiers: chr4:g.188345333G>C (hg19) ; chr4:g.187424179G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.187424179G>C , CM000666.2:g.187424179G>C	GRCh38
NC_000004.11:g.188345333G>C , CM000666.1:g.188345333G>C	GRCh37
NC_000004.10:g.188582327G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038931.1:n.322+81113C>G
XR_939603.1:n.268+1182G>C
XR_001741954.1:n.258+10468G>C
XR_001741955.1:n.1517+1182G>C
XR_001741956.1:n.258+10468G>C
XR_939603.2:n.269+1182G>C