Canonical Allele Identifier: CA466833074

Gene: LINC02977

Linked Data

• dbSNP Id: rs185612999
• gnomAD v3: 9-112035775-A-G
• gnomAD v4: 9-112035775-A-G
• MyVariant Identifiers: chr9:g.114798055A>G (hg19) ; chr9:g.112035775A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.112035775A>G , CM000671.2:g.112035775A>G	GRCh38
NC_000009.11:g.114798055A>G , CM000671.1:g.114798055A>G	GRCh37
NC_000009.10:g.113837876A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930251.3:n.2186+2404T>C