Canonical Allele Identifier: CA2601076584
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs2118504396

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261992C>G , CM000671.2:g.103261992C>G GRCh38
NC_000009.11:g.106024274C>G , CM000671.1:g.106024274C>G GRCh37
NC_000009.10:g.105064095C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2532G>C