Canonical Allele Identifier: CA111096859
Gene: LINC02268 HGNC NCBI

Linked Data

dbSNP Id: rs759880955
gnomAD v2: 4-175027476-C-G
gnomAD v3: 4-174106325-C-G
gnomAD v4: 4-174106325-C-G
MyVariant Identifiers: chr4:g.175027476C>G (hg19) chr4:g.174106325C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.174106325C>G , CM000666.2:g.174106325C>G GRCh38
NC_000004.11:g.175027476C>G , CM000666.1:g.175027476C>G GRCh37
NC_000004.10:g.175264051C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125896.1:n.276-8496G>C
XR_939484.1:n.877+18686C>G
XR_939485.1:n.877+18686C>G
Search 100 bp 5'
Search 100 bp 3'