Canonical Allele Identifier: CA198811533

Gene: LINC02977

Linked Data

• dbSNP Id: rs1048837147
• MyVariant Identifiers: chr9:g.114798057T>G (hg19) ; chr9:g.112035777T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.112035777T>G , CM000671.2:g.112035777T>G	GRCh38
NC_000009.11:g.114798057T>G , CM000671.1:g.114798057T>G	GRCh37
NC_000009.10:g.113837878T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930251.3:n.2186+2402A>C