Canonical Allele Identifier: CA198811530

Gene: LINC02977

Linked Data

• dbSNP Id: rs10125054
• gnomAD v2: 9-114798037-G-A
• gnomAD v3: 9-112035757-G-A
• gnomAD v4: 9-112035757-G-A
• MyVariant Identifiers: chr9:g.114798037G>A (hg19) ; chr9:g.112035757G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
XR_930251.3:n.2186+2422C>T