Canonical Allele Identifier: CA914598637
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1568576788
gnomAD v2: 20-22050607-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069969C>T , CM000682.2:g.22069969C>T GRCh38
NC_000020.10:g.22050607C>T , CM000682.1:g.22050607C>T GRCh37
NC_000020.9:g.21998607C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.445+1281C>T
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