Canonical Allele Identifier: CA857924160
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1246252062
MyVariant Identifiers: chr9:g.106024033G>A (hg19) chr9:g.103261751G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261751G>A , CM000671.2:g.103261751G>A GRCh38
NC_000009.11:g.106024033G>A , CM000671.1:g.106024033G>A GRCh37
NC_000009.10:g.105063854G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2773C>T
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