Canonical Allele Identifier: CA197961781
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs375761663

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261856del , CM000671.2:g.103261856del GRCh38
NC_000009.11:g.106024138del , CM000671.1:g.106024138del GRCh37
NC_000009.10:g.105063959del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2669del