ClinGen Allele Registry
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Canonical Allele Identifier:
CA113752061
Gene: LINC02145
HGNC
NCBI
Linked Data
dbSNP Id:
rs12518614
gnomAD v2:
5-6324293-A-G
gnomAD v3:
5-6324180-A-G
gnomAD v4:
5-6324180-A-G
MyVariant Identifiers:
chr5:g.6324293A>G (hg19)
chr5:g.6324180A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.6324180A>G , CM000667.2:g.6324180A>G
GRCh38
NC_000005.9:g.6324293A>G , CM000667.1:g.6324293A>G
GRCh37
NC_000005.8:g.6377293A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_028351.1:n.144-11464T>C
Search 100 bp 5'
Search 100 bp 3'