Canonical Allele Identifier: CA1872767444
Gene: LINC02977 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
XR_930251.3:n.2186+2606G=