Canonical Allele Identifier: CA466833064
Gene: LINC02977 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.114798051A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.112035771A>T , CM000671.2:g.112035771A>T GRCh38
NC_000009.11:g.114798051A>T , CM000671.1:g.114798051A>T GRCh37
NC_000009.10:g.113837872A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930251.3:n.2186+2408T>A