Canonical Allele Identifier: CA113752066
Gene: LINC02145 HGNC NCBI

Linked Data

dbSNP Id: rs140751402
gnomAD v3: 5-6324183-C-T
gnomAD v4: 5-6324183-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324183C>T , CM000667.2:g.6324183C>T GRCh38
NC_000005.9:g.6324296C>T , CM000667.1:g.6324296C>T GRCh37
NC_000005.8:g.6377296C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028351.1:n.144-11467G>A