Canonical Allele Identifier: CA635117072
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1281689713
gnomAD v2: 20-22050307-T-C
gnomAD v3: 20-22069669-T-C
gnomAD v4: 20-22069669-T-C
MyVariant Identifiers: chr20:g.22050307T>C (hg19) chr20:g.22069669T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069669T>C , CM000682.2:g.22069669T>C GRCh38
NC_000020.10:g.22050307T>C , CM000682.1:g.22050307T>C GRCh37
NC_000020.9:g.21998307T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+981T>C
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Search 100 bp 3'