ClinGen Allele Registry
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Canonical Allele Identifier:
CA1693197801
Gene: LINC01162
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.20845396C= , CM000669.2:g.20845396C=
GRCh38
NC_000007.13:g.20885015C= , CM000669.1:g.20885015C=
GRCh37
NC_000007.12:g.20851540C=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_126381.1:n.74+9892C=
Search 100 bp 5'
Search 100 bp 3'