Canonical Allele Identifier: CA466833021

Gene: LINC02977

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.112035757G>C , CM000671.2:g.112035757G>C	GRCh38
NC_000009.11:g.114798037G>C , CM000671.1:g.114798037G>C	GRCh37
NC_000009.10:g.113837858G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930251.3:n.2186+2422C>G