Canonical Allele Identifier: CA1597811819
Gene: LINC03000 HGNC NCBI

Linked Data

dbSNP Id: rs10515889

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.165119891A>T , CM000667.2:g.165119891A>T GRCh38
NC_000005.9:g.164546897A>T , CM000667.1:g.164546897A>T GRCh37
NC_000005.8:g.164479475A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941179.1:n.357-51487A>T