Canonical Allele Identifier: CA1072866631
Gene: LINC02145 HGNC NCBI

Linked Data

dbSNP Id: rs1737040503
gnomAD v3: 5-6324088-A-C
gnomAD v4: 5-6324088-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324088A>C , CM000667.2:g.6324088A>C GRCh38
NC_000005.9:g.6324201A>C , CM000667.1:g.6324201A>C GRCh37
NC_000005.8:g.6377201A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028351.1:n.144-11372T>G