Canonical Allele Identifier: CA299441752

Gene: LINC00907

Linked Data

• dbSNP Id: rs550457478
• gnomAD v2: 18-40050436-G-A
• gnomAD v3: 18-42470471-G-A
• gnomAD v4: 18-42470471-G-A
• MyVariant Identifiers: chr18:g.40050436G>A (hg19) ; chr18:g.42470471G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.42470471G>A , CM000680.2:g.42470471G>A	GRCh38
NC_000018.9:g.40050436G>A , CM000680.1:g.40050436G>A	GRCh37
NC_000018.8:g.38304434G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046174.2:n.872+15482G>A
NR_046454.1:n.652+15482G>A
NR_046455.1:n.489+15482G>A