Canonical Allele Identifier: CA126242386
Gene: LINC02208 HGNC NCBI

Linked Data

dbSNP Id: rs531380712
gnomAD v2: 5-117701426-G-GTT
gnomAD v3: 5-118365731-G-GTT
gnomAD v4: 5-118365731-G-GTT
MyVariant Identifiers: chr5:g.117701426_117701427insTT (hg19) chr5:g.118365731_118365732insTT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365731_118365732insTT , CM000667.2:g.118365731_118365732insTT GRCh38
NC_000005.9:g.117701426_117701427insTT , CM000667.1:g.117701426_117701427insTT GRCh37
NC_000005.8:g.117729325_117729326insTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14225_2658-14224insAA
Search 100 bp 5'
Search 100 bp 3'