Canonical Allele Identifier: CA302041033
Gene: LINC01924 HGNC NCBI

Linked Data

dbSNP Id: rs114420826
gnomAD v2: 18-61877056-G-T
gnomAD v3: 18-64209821-G-T
gnomAD v4: 18-64209821-G-T
MyVariant Identifiers: chr18:g.61877056G>T (hg19) chr18:g.64209821G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.64209821G>T , CM000680.2:g.64209821G>T GRCh38
NC_000018.9:g.61877056G>T , CM000680.1:g.61877056G>T GRCh37
NC_000018.8:g.60028036G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033881.1:n.201-39480G>T
Search 100 bp 5'
Search 100 bp 3'