Canonical Allele Identifier: CA466833078

Gene: LINC02977

Linked Data

• dbSNP Id: rs1199057760
• gnomAD v3: 9-112035776-C-T
• gnomAD v4: 9-112035776-C-T
• MyVariant Identifiers: chr9:g.114798056C>T (hg19) ; chr9:g.112035776C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.112035776C>T , CM000671.2:g.112035776C>T	GRCh38
NC_000009.11:g.114798056C>T , CM000671.1:g.114798056C>T	GRCh37
NC_000009.10:g.113837877C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930251.3:n.2186+2403G>A