Canonical Allele Identifier: CA812941149

Gene: LINC02145

Linked Data

• dbSNP Id: rs1171748015
• gnomAD v3: 5-6324203-C-T
• gnomAD v4: 5-6324203-C-T
• MyVariant Identifiers: chr5:g.6324316C>T (hg19) ; chr5:g.6324203C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6324203C>T , CM000667.2:g.6324203C>T	GRCh38
NC_000005.9:g.6324316C>T , CM000667.1:g.6324316C>T	GRCh37
NC_000005.8:g.6377316C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_028351.1:n.144-11487G>A