Canonical Allele Identifier: CA2590604431
Gene: LINC01432 HGNC NCBI

Linked Data

gnomAD v3: 20-22070146-C-G
gnomAD v4: 20-22070146-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070146C>G , CM000682.2:g.22070146C>G GRCh38
NC_000020.10:g.22050784C>G , CM000682.1:g.22050784C>G GRCh37
NC_000020.9:g.21998784C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1458C>G
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