Canonical Allele Identifier: CA466833079
Gene: LINC02977 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.114798057T>A (hg19)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
XR_930251.3:n.2186+2402A>T
Search 100 bp 5'
Search 100 bp 3'