Canonical Allele Identifier: CA2736614716
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs2122510279

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22059277A>C , CM000682.2:g.22059277A>C GRCh38
NC_000020.10:g.22039915A>C , CM000682.1:g.22039915A>C GRCh37
NC_000020.9:g.21987915A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.195+4993A>C