Canonical Allele Identifier: CA2597380960

Gene: LINC00333

Linked Data

• dbSNP Id: rs2137120057
• gnomAD v3: 13-84458248-C-T
• gnomAD v4: 13-84458248-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.84458248C>T , CM000675.2:g.84458248C>T	GRCh38
NC_000013.10:g.85032383C>T , CM000675.1:g.85032383C>T	GRCh37
NC_000013.9:g.83930384C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_046871.1:n.139-104116C>T
XR_942133.1:n.369-46329G>A
XR_942134.1:n.366-46329G>A