Canonical Allele Identifier: CA557804994

Gene: LINC02145

Linked Data

• dbSNP Id: rs1159372896
• gnomAD v2: 5-6324234-G-A
• gnomAD v3: 5-6324121-G-A
• gnomAD v4: 5-6324121-G-A
• MyVariant Identifiers: chr5:g.6324234G>A (hg19) ; chr5:g.6324121G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6324121G>A , CM000667.2:g.6324121G>A	GRCh38
NC_000005.9:g.6324234G>A , CM000667.1:g.6324234G>A	GRCh37
NC_000005.8:g.6377234G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_028351.1:n.144-11405C>T