Canonical Allele Identifier: CA589962168
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1313600240
gnomAD v2: 9-106023985-A-C
gnomAD v3: 9-103261703-A-C
gnomAD v4: 9-103261703-A-C
MyVariant Identifiers: chr9:g.106023985A>C (hg19) chr9:g.103261703A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261703A>C , CM000671.2:g.103261703A>C GRCh38
NC_000009.11:g.106023985A>C , CM000671.1:g.106023985A>C GRCh37
NC_000009.10:g.105063806A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2821T>G
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