ClinGen Allele Registry
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Canonical Allele Identifier:
CA1693234781
Gene: LINC01162
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.20954825T= , CM000669.2:g.20954825T=
GRCh38
NC_000007.13:g.20994444T= , CM000669.1:g.20994444T=
GRCh37
NC_000007.12:g.20960969T=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_126381.1:n.152-66043T=
Search 100 bp 5'
Search 100 bp 3'