Canonical Allele Identifier: CA2718679509
Gene: LINC02055 HGNC NCBI

Linked Data

dbSNP Id: rs2130353127
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.136837697G>A , CM000670.2:g.136837697G>A GRCh38
NC_000008.10:g.137849940G>A , CM000670.1:g.137849940G>A GRCh37
NC_000008.9:g.137919122G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147196.1:n.443+40327G>A
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