Canonical Allele Identifier: CA197961822
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs995275532

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261994G>T , CM000671.2:g.103261994G>T GRCh38
NC_000009.11:g.106024276G>T , CM000671.1:g.106024276G>T GRCh37
NC_000009.10:g.105064097G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2530C>A