Canonical Allele Identifier: CA701182642
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs1376718152
gnomAD v3: 13-78836356-A-G
gnomAD v4: 13-78836356-A-G
MyVariant Identifiers: chr13:g.79410491A>G (hg19) chr13:g.78836356A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836356A>G , CM000675.2:g.78836356A>G GRCh38
NC_000013.10:g.79410491A>G , CM000675.1:g.79410491A>G GRCh37
NC_000013.9:g.78308492A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046869.2:n.111+3584T>C
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