Canonical Allele Identifier: CA113752020

Gene: LINC02145

Linked Data

• dbSNP Id: rs968534242
• gnomAD v2: 5-6324202-A-G
• gnomAD v3: 5-6324089-A-G
• gnomAD v4: 5-6324089-A-G
• MyVariant Identifiers: chr5:g.6324202A>G (hg19) ; chr5:g.6324089A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6324089A>G , CM000667.2:g.6324089A>G	GRCh38
NC_000005.9:g.6324202A>G , CM000667.1:g.6324202A>G	GRCh37
NC_000005.8:g.6377202A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_028351.1:n.144-11373T>C