Canonical Allele Identifier: CA466833022
Gene: LINC02977 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.114798037G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.112035757G>T , CM000671.2:g.112035757G>T GRCh38
NC_000009.11:g.114798037G>T , CM000671.1:g.114798037G>T GRCh37
NC_000009.10:g.113837858G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930251.3:n.2186+2422C>A