Canonical Allele Identifier: CA113752071

Gene: LINC02145

Linked Data

• dbSNP Id: rs781076540
• MyVariant Identifiers: chr5:g.6324314G>T (hg19) ; chr5:g.6324201G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6324201G>T , CM000667.2:g.6324201G>T	GRCh38
NC_000005.9:g.6324314G>T , CM000667.1:g.6324314G>T	GRCh37
NC_000005.8:g.6377314G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_028351.1:n.144-11485C>A