Canonical Allele Identifier: CA113752123
Gene: LINC02145 HGNC NCBI

Linked Data

dbSNP Id: rs368161976
gnomAD v2: 5-6324333-T-C
gnomAD v3: 5-6324220-T-C
gnomAD v4: 5-6324220-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324220T>C , CM000667.2:g.6324220T>C GRCh38
NC_000005.9:g.6324333T>C , CM000667.1:g.6324333T>C GRCh37
NC_000005.8:g.6377333T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028351.1:n.144-11504A>G