Canonical Allele Identifier: CA611135015
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs1445285317
gnomAD v2: 13-79410552-G-T
gnomAD v3: 13-78836417-G-T
gnomAD v4: 13-78836417-G-T
MyVariant Identifiers: chr13:g.79410552G>T (hg19) chr13:g.78836417G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836417G>T , CM000675.2:g.78836417G>T GRCh38
NC_000013.10:g.79410552G>T , CM000675.1:g.79410552G>T GRCh37
NC_000013.9:g.78308553G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046869.2:n.111+3523C>A
Search 100 bp 5'
Search 100 bp 3'