ClinGen Allele Registry
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Canonical Allele Identifier:
CA1869205494
Gene: LINC01492
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.103262019A= , CM000671.2:g.103262019A=
GRCh38
NC_000009.11:g.106024301A= , CM000671.1:g.106024301A=
GRCh37
NC_000009.10:g.105064122A=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_121578.1:n.771+2505T=
Search 100 bp 5'
Search 100 bp 3'