Canonical Allele Identifier: CA1872767542
Gene: LINC02977 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.112035776C= , CM000671.2:g.112035776C= GRCh38
NC_000009.11:g.114798056C= , CM000671.1:g.114798056C= GRCh37
NC_000009.10:g.113837877C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930251.3:n.2186+2403G=