Canonical Allele Identifier: CA716206648
Gene: LINC01418 HGNC NCBI

Linked Data

dbSNP Id: rs77963519
gnomAD v3: 15-81901505-G-C
gnomAD v4: 15-81901505-G-C
MyVariant Identifiers: chr15:g.82193846G>C (hg19) chr15:g.81901505G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.81901505G>C , CM000677.2:g.81901505G>C GRCh38
NC_000015.9:g.82193846G>C , CM000677.1:g.82193846G>C GRCh37
NC_000015.8:g.79980901G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001751639.1:n.734+13842C>G
XR_001751640.1:n.623+24168C>G
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