Canonical Allele Identifier: CA253224646
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs553820440
gnomAD v2: 13-79410636-AAG-A
gnomAD v3: 13-78836501-AAG-A
gnomAD v4: 13-78836501-AAG-A
MyVariant Identifiers: chr13:g.79410637_79410638del (hg19) chr13:g.78836502_78836503del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836504_78836505del , CM000675.2:g.78836504_78836505del GRCh38
NC_000013.10:g.79410639_79410640del , CM000675.1:g.79410639_79410640del GRCh37
NC_000013.9:g.78308640_78308641del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046869.2:n.111+3437_111+3438del
Search 100 bp 5'
Search 100 bp 3'