Canonical Allele Identifier: CA2309139595
Gene: LINC01924 HGNC NCBI

Linked Data

dbSNP Id: rs2051786240
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.64209831A>T , CM000680.2:g.64209831A>T GRCh38
NC_000018.9:g.61877066A>T , CM000680.1:g.61877066A>T GRCh37
NC_000018.8:g.60028046A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033881.1:n.201-39470A>T
Search 100 bp 5'
Search 100 bp 3'