Canonical Allele Identifier: CA1872767450
Gene: LINC02977 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.112035580A= , CM000671.2:g.112035580A= GRCh38
NC_000009.11:g.114797860A= , CM000671.1:g.114797860A= GRCh37
NC_000009.10:g.113837681A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930251.3:n.2186+2599T=