ClinGen Allele Registry
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Canonical Allele Identifier:
CA1055324297
Gene: LINC00880
HGNC
NCBI
Linked Data
gnomAD v3:
3-157119190-C-A
gnomAD v4:
3-157119190-C-A
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.157119190C>A , CM000665.2:g.157119190C>A
GRCh38
NC_000003.11:g.156836979C>A , CM000665.1:g.156836979C>A
GRCh37
NC_000003.10:g.158319673C>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_034007.1:n.127+3686G>T
Search 100 bp 5'
Search 100 bp 3'