Canonical Allele Identifier: CA16337351
Gene: LINC01299 HGNC NCBI

Linked Data

dbSNP Id: rs6981992
gnomAD v2: 8-66463478-G-T
gnomAD v3: 8-65551243-G-T
gnomAD v4: 8-65551243-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.65551243G>T , CM000670.2:g.65551243G>T GRCh38
NC_000008.10:g.66463478G>T , CM000670.1:g.66463478G>T GRCh37
NC_000008.9:g.66626032G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033893.1:n.61+11363C>A