Canonical Allele Identifier: CA16091918
Gene: LINC01830 HGNC NCBI

Linked Data

dbSNP Id: rs17043947
gnomAD v2: 2-22736987-C-T
gnomAD v3: 2-22514115-C-T
gnomAD v4: 2-22514115-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.22514115C>T , CM000664.2:g.22514115C>T GRCh38
NC_000002.11:g.22736987C>T , CM000664.1:g.22736987C>T GRCh37
NC_000002.10:g.22590492C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939817.1:n.182+16921G>A
XR_002959374.1:n.249+16921G>A