Canonical Allele Identifier: CA1072866680
Gene: LINC02145 HGNC NCBI

Linked Data

dbSNP Id: rs1737043106
gnomAD v3: 5-6324198-CT-C
gnomAD v4: 5-6324198-CT-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324199del , CM000667.2:g.6324199del GRCh38
NC_000005.9:g.6324312del , CM000667.1:g.6324312del GRCh37
NC_000005.8:g.6377312del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028351.1:n.144-11483del