Canonical Allele Identifier: CA466833032
Gene: LINC02977 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.114798041G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.112035761G>A , CM000671.2:g.112035761G>A GRCh38
NC_000009.11:g.114798041G>A , CM000671.1:g.114798041G>A GRCh37
NC_000009.10:g.113837862G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930251.3:n.2186+2418C>T