Canonical Allele Identifier: CA466833073

Gene: LINC02977

Linked Data

• MyVariant Identifiers: chr9:g.114798054C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.112035774C>T , CM000671.2:g.112035774C>T	GRCh38
NC_000009.11:g.114798054C>T , CM000671.1:g.114798054C>T	GRCh37
NC_000009.10:g.113837875C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930251.3:n.2186+2405G>A