Canonical Allele Identifier: CA1869205445
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1827341530
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261912C>A , CM000671.2:g.103261912C>A GRCh38
NC_000009.11:g.106024194C>A , CM000671.1:g.106024194C>A GRCh37
NC_000009.10:g.105064015C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2612G>T
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Search 100 bp 3'