Canonical Allele Identifier: CA573568041

Gene: LINC02981

Linked Data

• dbSNP Id: rs1393613238
• gnomAD v2: 7-26481817-T-G
• gnomAD v3: 7-26442197-T-G
• gnomAD v4: 7-26442197-T-G
• MyVariant Identifiers: chr7:g.26481817T>G (hg19) ; chr7:g.26442197T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.26442197T>G , CM000669.2:g.26442197T>G	GRCh38
NC_000007.13:g.26481817T>G , CM000669.1:g.26481817T>G	GRCh37
NC_000007.12:g.26448342T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011515671.1:c.336-18169T>G	XP_011513973.1:n.336-18169T>G
NR_148499.1:n.630+29958T>G
NR_148500.1:n.225+29958T>G
NR_148501.1:n.508+29958T>G
NR_148502.1:n.453+43176T>G
NR_148503.1:n.630+29958T>G
NR_148504.1:n.630+29958T>G