Canonical Allele Identifier: CA466832515

Gene: LINC02977

Linked Data

• MyVariant Identifiers: chr9:g.114797863A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.112035583A>T , CM000671.2:g.112035583A>T	GRCh38
NC_000009.11:g.114797863A>T , CM000671.1:g.114797863A>T	GRCh37
NC_000009.10:g.113837684A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_930251.3:n.2186+2596T>A