Canonical Allele Identifier: CA812941090

Gene: LINC02145

Linked Data

• dbSNP Id: rs1282870855
• MyVariant Identifiers: chr5:g.6324251T>C (hg19) ; chr5:g.6324138T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6324138T>C , CM000667.2:g.6324138T>C	GRCh38
NC_000005.9:g.6324251T>C , CM000667.1:g.6324251T>C	GRCh37
NC_000005.8:g.6377251T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_028351.1:n.144-11422A>G