Canonical Allele Identifier: CA2720273885
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs2118504184
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261814T>G , CM000671.2:g.103261814T>G GRCh38
NC_000009.11:g.106024096T>G , CM000671.1:g.106024096T>G GRCh37
NC_000009.10:g.105063917T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2710A>C
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