Canonical Allele Identifier: CA779420776

Gene: LINC00907

Linked Data

• dbSNP Id: rs1226396991
• MyVariant Identifiers: chr18:g.40050266_40050267insA (hg19) ; chr18:g.42470301_42470302insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.42470304dup , CM000680.2:g.42470304dup	GRCh38
NC_000018.9:g.40050269dup , CM000680.1:g.40050269dup	GRCh37
NC_000018.8:g.38304267dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046174.2:n.872+15315dup
NR_046454.1:n.652+15315dup
NR_046455.1:n.489+15315dup