Canonical Allele Identifier: CA112636663

Gene: LINC02515

Linked Data

• dbSNP Id: rs927479213
• MyVariant Identifiers: chr4:g.188345279A>G (hg19) ; chr4:g.187424125A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.187424125A>G , CM000666.2:g.187424125A>G	GRCh38
NC_000004.11:g.188345279A>G , CM000666.1:g.188345279A>G	GRCh37
NC_000004.10:g.188582273A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038931.1:n.322+81167T>C
XR_939603.1:n.268+1128A>G
XR_001741954.1:n.258+10414A>G
XR_001741955.1:n.1517+1128A>G
XR_001741956.1:n.258+10414A>G
XR_939603.2:n.269+1128A>G