Canonical Allele Identifier: CA2736614193
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs2122508113

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22057049T>C , CM000682.2:g.22057049T>C GRCh38
NC_000020.10:g.22037687T>C , CM000682.1:g.22037687T>C GRCh37
NC_000020.9:g.21985687T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.195+2765T>C