Canonical Allele Identifier: CA629642771
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1213717012

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470343T>C , CM000680.2:g.42470343T>C GRCh38
NC_000018.9:g.40050308T>C , CM000680.1:g.40050308T>C GRCh37
NC_000018.8:g.38304306T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046174.2:n.872+15354T>C
NR_046454.1:n.652+15354T>C
NR_046455.1:n.489+15354T>C