ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA557805000
Gene: LINC02145
HGNC
NCBI
Linked Data
dbSNP Id:
rs1240210095
gnomAD v2:
5-6324335-T-C
gnomAD v3:
5-6324222-T-C
gnomAD v4:
5-6324222-T-C
MyVariant Identifiers:
chr5:g.6324335T>C (hg19)
chr5:g.6324222T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.6324222T>C , CM000667.2:g.6324222T>C
GRCh38
NC_000005.9:g.6324335T>C , CM000667.1:g.6324335T>C
GRCh37
NC_000005.8:g.6377335T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_028351.1:n.144-11506A>G
Search 100 bp 5'
Search 100 bp 3'