Canonical Allele Identifier: CA1822904774
Gene: LINC02055 HGNC NCBI

Linked Data

dbSNP Id: rs1814973966

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.136837668A>G , CM000670.2:g.136837668A>G GRCh38
NC_000008.10:g.137849911A>G , CM000670.1:g.137849911A>G GRCh37
NC_000008.9:g.137919093A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147196.1:n.443+40298A>G