Canonical Allele Identifier: CA1869205514
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1827343568

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103262054T>C , CM000671.2:g.103262054T>C GRCh38
NC_000009.11:g.106024336T>C , CM000671.1:g.106024336T>C GRCh37
NC_000009.10:g.105064157T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2470A>G