Canonical Allele Identifier: CA466832732
Gene: LINC02977 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.114797939G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.112035659G>C , CM000671.2:g.112035659G>C GRCh38
NC_000009.11:g.114797939G>C , CM000671.1:g.114797939G>C GRCh37
NC_000009.10:g.113837760G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930251.3:n.2186+2520C>G