Canonical Allele Identifier: CA198811522
Gene: LINC02977 HGNC NCBI

Linked Data

dbSNP Id: rs985910540

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.112035658G>T , CM000671.2:g.112035658G>T GRCh38
NC_000009.11:g.114797938G>T , CM000671.1:g.114797938G>T GRCh37
NC_000009.10:g.113837759G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930251.3:n.2186+2521C>A