Canonical Allele Identifier: CA1869205444
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1827341503
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261911G>T , CM000671.2:g.103261911G>T GRCh38
NC_000009.11:g.106024193G>T , CM000671.1:g.106024193G>T GRCh37
NC_000009.10:g.105064014G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2613C>A
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