Canonical Allele Identifier: CA1080614521
Gene: LINC02147 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118002058G>C , CM000667.2:g.118002058G>C GRCh38
NC_000005.9:g.117337753G>C , CM000667.1:g.117337753G>C GRCh37
NC_000005.8:g.117365652G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104997.1:n.170+76927G>C
Search 100 bp 5'
Search 100 bp 3'