Canonical Allele Identifier: CA466832731
Gene: LINC02977 HGNC NCBI

Linked Data

dbSNP Id: rs1406263189

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.112035659G>T , CM000671.2:g.112035659G>T GRCh38
NC_000009.11:g.114797939G>T , CM000671.1:g.114797939G>T GRCh37
NC_000009.10:g.113837760G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930251.3:n.2186+2520C>A