Canonical Allele Identifier: CA197961812
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs545243129

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261944T>G , CM000671.2:g.103261944T>G GRCh38
NC_000009.11:g.106024226T>G , CM000671.1:g.106024226T>G GRCh37
NC_000009.10:g.105064047T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2580A>C