Canonical Allele Identifier: CA1099576868

Gene: LINC02981

Linked Data

• dbSNP Id: rs1782324513
• gnomAD v3: 7-26442227-T-C
• gnomAD v4: 7-26442227-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.26442227T>C , CM000669.2:g.26442227T>C	GRCh38
NC_000007.13:g.26481847T>C , CM000669.1:g.26481847T>C	GRCh37
NC_000007.12:g.26448372T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011515671.1:c.336-18139T>C	XP_011513973.1:n.336-18139T>C
NR_148499.1:n.630+29988T>C
NR_148500.1:n.225+29988T>C
NR_148501.1:n.508+29988T>C
NR_148502.1:n.453+43206T>C
NR_148503.1:n.630+29988T>C
NR_148504.1:n.630+29988T>C