Canonical Allele Identifier: CA2708089263
Gene: LINC02145 HGNC NCBI

Linked Data

dbSNP Id: rs2111393782
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324253C>A , CM000667.2:g.6324253C>A GRCh38
NC_000005.9:g.6324366C>A , CM000667.1:g.6324366C>A GRCh37
NC_000005.8:g.6377366C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_028351.1:n.144-11537G>T
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