Canonical Allele Identifier: CA113752142
Gene: LINC02145 HGNC NCBI

Linked Data

dbSNP Id: rs1003140820

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324258G>C , CM000667.2:g.6324258G>C GRCh38
NC_000005.9:g.6324371G>C , CM000667.1:g.6324371G>C GRCh37
NC_000005.8:g.6377371G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028351.1:n.144-11542C>G