Canonical Allele Identifier: CA251061671
Gene: LINC01442 HGNC NCBI

Linked Data

dbSNP Id: rs7337573

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.60939535T>C , CM000675.2:g.60939535T>C GRCh38
NC_000013.10:g.61513669T>C , CM000675.1:g.61513669T>C GRCh37
NC_000013.9:g.60411670T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749887.1:n.183-872T>C
XR_001749888.1:n.239-872T>C
XR_001749889.1:n.183T>C