Canonical Allele Identifier: CA466833072
Gene: LINC02977 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
XR_930251.3:n.2186+2405G>C