Canonical Allele Identifier: CA466832486
Gene: LINC02977 HGNC NCBI

Linked Data

dbSNP Id: rs1589558191
MyVariant Identifiers: chr9:g.114797853C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.112035573C>T , CM000671.2:g.112035573C>T GRCh38
NC_000009.11:g.114797853C>T , CM000671.1:g.114797853C>T GRCh37
NC_000009.10:g.113837674C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930251.3:n.2186+2606G>A