Canonical Allele Identifier: CA2558682361
Gene: LINC01492 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103262099G>T , CM000671.2:g.103262099G>T GRCh38
NC_000009.11:g.106024381G>T , CM000671.1:g.106024381G>T GRCh37
NC_000009.10:g.105064202G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2425C>A
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