Canonical Allele Identifier: CA779420922

Gene: LINC00907

Linked Data

• dbSNP Id: rs72907045
• gnomAD v3: 18-42470534-T-A
• gnomAD v4: 18-42470534-T-A
• MyVariant Identifiers: chr18:g.40050499T>A (hg19) ; chr18:g.42470534T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.42470534T>A , CM000680.2:g.42470534T>A	GRCh38
NC_000018.9:g.40050499T>A , CM000680.1:g.40050499T>A	GRCh37
NC_000018.8:g.38304497T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046174.2:n.872+15545T>A
NR_046454.1:n.652+15545T>A
NR_046455.1:n.489+15545T>A