Canonical Allele Identifier: CA466832755
Gene: LINC02977 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.114797947A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.112035667A>C , CM000671.2:g.112035667A>C GRCh38
NC_000009.11:g.114797947A>C , CM000671.1:g.114797947A>C GRCh37
NC_000009.10:g.113837768A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930251.3:n.2186+2512T>G