Canonical Allele Identifier: CA1110700075

Gene: LINC00208

Linked Data

• dbSNP Id: rs1802027864
• gnomAD v3: 8-11577951-T-C
• gnomAD v4: 8-11577951-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577951T>C , CM000670.2:g.11577951T>C	GRCh38
NC_000008.10:g.11435460T>C , CM000670.1:g.11435460T>C	GRCh37
NC_000008.9:g.11472869T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_040035.1:n.784-419T>C