Canonical Allele Identifier: CA1872767546
Gene: LINC02977 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.112035777T= , CM000671.2:g.112035777T= GRCh38
NC_000009.11:g.114798057T= , CM000671.1:g.114798057T= GRCh37
NC_000009.10:g.113837878T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930251.3:n.2186+2402A=