Canonical Allele Identifier: CA198811513
Gene: LINC02977 HGNC NCBI

Linked Data

dbSNP Id: rs887809619
MyVariant Identifiers: chr9:g.114797866A>C (hg19) chr9:g.112035586A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.112035586A>C , CM000671.2:g.112035586A>C GRCh38
NC_000009.11:g.114797866A>C , CM000671.1:g.114797866A>C GRCh37
NC_000009.10:g.113837687A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930251.3:n.2186+2593T>G
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