Canonical Allele Identifier: CA1127548497
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1827342757

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261990C>A , CM000671.2:g.103261990C>A GRCh38
NC_000009.11:g.106024272C>A , CM000671.1:g.106024272C>A GRCh37
NC_000009.10:g.105064093C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2534G>T