Canonical Allele Identifier: CA299441742

Gene: LINC00907

Linked Data

• dbSNP Id: rs940551447
• gnomAD v3: 18-42470384-T-C
• gnomAD v4: 18-42470384-T-C
• MyVariant Identifiers: chr18:g.40050349T>C (hg19) ; chr18:g.42470384T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.42470384T>C , CM000680.2:g.42470384T>C	GRCh38
NC_000018.9:g.40050349T>C , CM000680.1:g.40050349T>C	GRCh37
NC_000018.8:g.38304347T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046174.2:n.872+15395T>C
NR_046454.1:n.652+15395T>C
NR_046455.1:n.489+15395T>C