Canonical Allele Identifier: CA2592729401

Gene: LINC00208

Linked Data

• dbSNP Id: rs2117643817
• gnomAD v3: 8-11577869-C-T
• gnomAD v4: 8-11577869-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577869C>T , CM000670.2:g.11577869C>T	GRCh38
NC_000008.10:g.11435378C>T , CM000670.1:g.11435378C>T	GRCh37
NC_000008.9:g.11472787C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040035.1:n.784-501C>T