Canonical Allele Identifier: CA113752123

Gene: LINC02145

Linked Data

• dbSNP Id: rs368161976
• gnomAD v2: 5-6324333-T-C
• gnomAD v3: 5-6324220-T-C
• gnomAD v4: 5-6324220-T-C
• MyVariant Identifiers: chr5:g.6324333T>C (hg19) ; chr5:g.6324220T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6324220T>C , CM000667.2:g.6324220T>C	GRCh38
NC_000005.9:g.6324333T>C , CM000667.1:g.6324333T>C	GRCh37
NC_000005.8:g.6377333T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_028351.1:n.144-11504A>G