Canonical Allele Identifier: CA197961794
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs755061909

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261877C>T , CM000671.2:g.103261877C>T GRCh38
NC_000009.11:g.106024159C>T , CM000671.1:g.106024159C>T GRCh37
NC_000009.10:g.105063980C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2647G>A