Canonical Allele Identifier: CA562420263
Gene: LINC02208 HGNC NCBI

Linked Data

dbSNP Id: rs1198928475
gnomAD v2: 5-117701478-A-C
gnomAD v3: 5-118365783-A-C
gnomAD v4: 5-118365783-A-C
MyVariant Identifiers: chr5:g.117701478A>C (hg19) chr5:g.118365783A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365783A>C , CM000667.2:g.118365783A>C GRCh38
NC_000005.9:g.117701478A>C , CM000667.1:g.117701478A>C GRCh37
NC_000005.8:g.117729377A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14276T>G
Search 100 bp 5'
Search 100 bp 3'