Canonical Allele Identifier: CA13302186

Gene: LINC02645

Linked Data

• dbSNP Id: rs729397
• gnomAD v2: 10-2532019-G-C
• gnomAD v3: 10-2489827-G-C
• gnomAD v4: 10-2489827-G-C
• MyVariant Identifiers: chr10:g.2532019G>C (hg19) ; chr10:g.2489827G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.2489827G>C , CM000672.2:g.2489827G>C	GRCh38
NC_000010.10:g.2532019G>C , CM000672.1:g.2532019G>C	GRCh37
NC_000010.9:g.2522019G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011519769.1:c.390+11731C>G	XP_011518071.1:n.390+11731C>G
XM_011519771.1:c.390+11731C>G	XP_011518073.1:n.390+11731C>G
XM_011519772.1:c.390+11731C>G	XP_011518074.1:n.390+11731C>G
XM_011519775.1:c.264+11857C>G	XP_011518077.1:n.264+11857C>G
XM_011519777.1:c.264+11857C>G	XP_011518079.1:n.264+11857C>G
XM_011519778.1:c.264+11857C>G	XP_011518080.1:n.264+11857C>G
NR_136146.1:n.89+11547C>G