Canonical Allele Identifier: CA26493373
Gene: LINC01725 HGNC NCBI

Linked Data

dbSNP Id: rs17129289
gnomAD v2: 1-84232748-T-C
gnomAD v3: 1-83767065-T-C
gnomAD v4: 1-83767065-T-C
MyVariant Identifiers: chr1:g.84232748T>C (hg19) chr1:g.83767065T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.83767065T>C , CM000663.2:g.83767065T>C GRCh38
NC_000001.10:g.84232748T>C , CM000663.1:g.84232748T>C GRCh37
NC_000001.9:g.84005336T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_119375.1:n.179-16766A>G
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