Canonical Allele Identifier: CA2539616488
Gene: LINC01492 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261931T>G , CM000671.2:g.103261931T>G GRCh38
NC_000009.11:g.106024213T>G , CM000671.1:g.106024213T>G GRCh37
NC_000009.10:g.105064034T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2593A>C
Search 100 bp 5'
Search 100 bp 3'