Canonical Allele Identifier: CA197961820
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs948812626

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261975T>C , CM000671.2:g.103261975T>C GRCh38
NC_000009.11:g.106024257T>C , CM000671.1:g.106024257T>C GRCh37
NC_000009.10:g.105064078T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2549A>G