Canonical Allele Identifier: CA1080647853
Gene: LINC02208 HGNC NCBI

Linked Data

dbSNP Id: rs542093031
gnomAD v3: 5-118365705-G-T
gnomAD v4: 5-118365705-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365705G>T , CM000667.2:g.118365705G>T GRCh38
NC_000005.9:g.117701400G>T , CM000667.1:g.117701400G>T GRCh37
NC_000005.8:g.117729299G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14198C>A
Search 100 bp 5'
Search 100 bp 3'