Canonical Allele Identifier: CA2718679233
Gene: LINC02055 HGNC NCBI

Linked Data

dbSNP Id: rs2130353115
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.136837686A>G , CM000670.2:g.136837686A>G GRCh38
NC_000008.10:g.137849929A>G , CM000670.1:g.137849929A>G GRCh37
NC_000008.9:g.137919111A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147196.1:n.443+40316A>G
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