ClinGen Allele Registry
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Canonical Allele Identifier:
CA557805001
Gene: LINC02145
HGNC
NCBI
Linked Data
dbSNP Id:
rs1348406122
gnomAD v2:
5-6324369-T-C
gnomAD v3:
5-6324256-T-C
gnomAD v4:
5-6324256-T-C
MyVariant Identifiers:
chr5:g.6324369T>C (hg19)
chr5:g.6324256T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.6324256T>C , CM000667.2:g.6324256T>C
GRCh38
NC_000005.9:g.6324369T>C , CM000667.1:g.6324369T>C
GRCh37
NC_000005.8:g.6377369T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_028351.1:n.144-11540A>G
Search 100 bp 5'
Search 100 bp 3'