Canonical Allele Identifier: CA113752111
Gene: LINC02145 HGNC NCBI

Linked Data

dbSNP Id: rs948430605
MyVariant Identifiers: chr5:g.6324332A>C (hg19) chr5:g.6324219A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324219A>C , CM000667.2:g.6324219A>C GRCh38
NC_000005.9:g.6324332A>C , CM000667.1:g.6324332A>C GRCh37
NC_000005.8:g.6377332A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_028351.1:n.144-11503T>G
Search 100 bp 5'
Search 100 bp 3'