Canonical Allele Identifier: CA557805000
Gene: LINC02145 HGNC NCBI

Linked Data

dbSNP Id: rs1240210095
gnomAD v2: 5-6324335-T-C
gnomAD v3: 5-6324222-T-C
gnomAD v4: 5-6324222-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324222T>C , CM000667.2:g.6324222T>C GRCh38
NC_000005.9:g.6324335T>C , CM000667.1:g.6324335T>C GRCh37
NC_000005.8:g.6377335T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028351.1:n.144-11506A>G