Canonical Allele Identifier: CA2298939940
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1907320456

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470583A>C , CM000680.2:g.42470583A>C GRCh38
NC_000018.9:g.40050548A>C , CM000680.1:g.40050548A>C GRCh37
NC_000018.8:g.38304546A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15594A>C
NR_046454.1:n.652+15594A>C
NR_046455.1:n.489+15594A>C