ClinGen Allele Registry
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Canonical Allele Identifier:
CA110561426
Gene: LINC02275
HGNC
NCBI
Linked Data
dbSNP Id:
rs11723530
gnomAD v2:
4-170880883-G-A
gnomAD v3:
4-169959732-G-A
gnomAD v4:
4-169959732-G-A
MyVariant Identifiers:
chr4:g.170880883G>A (hg19)
chr4:g.169959732G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.169959732G>A , CM000666.2:g.169959732G>A
GRCh38
NC_000004.11:g.170880883G>A , CM000666.1:g.170880883G>A
GRCh37
NC_000004.10:g.171117458G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_037878.1:n.87+16084C>T
Search 100 bp 5'
Search 100 bp 3'