Canonical Allele Identifier: CA1072866672
Gene: LINC02145 HGNC NCBI

Linked Data

dbSNP Id: rs1737042960
gnomAD v3: 5-6324184-AT-A
gnomAD v4: 5-6324184-AT-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324187del , CM000667.2:g.6324187del GRCh38
NC_000005.9:g.6324300del , CM000667.1:g.6324300del GRCh37
NC_000005.8:g.6377300del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028351.1:n.144-11469del