Canonical Allele Identifier: CA10773265
Gene: LINC02791 HGNC NCBI

Linked Data

dbSNP Id: rs4650135
gnomAD v2: 1-69684997-T-C
gnomAD v3: 1-69219314-T-C
gnomAD v4: 1-69219314-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.69219314T>C , CM000663.2:g.69219314T>C GRCh38
NC_000001.10:g.69684997T>C , CM000663.1:g.69684997T>C GRCh37
NC_000001.9:g.69457585T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_947483.1:n.314-3308A>G
XR_947484.1:n.103-3308A>G
XR_947485.1:n.314-2244A>G
XR_947486.1:n.864+881T>C
XR_001738105.1:n.374-3308A>G
XR_947483.3:n.344-3308A>G
XR_947486.2:n.891+881T>C