Canonical Allele Identifier: CA13817347
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs2184180
gnomAD v2: 13-79380816-T-G
gnomAD v3: 13-78806681-T-G
gnomAD v4: 13-78806681-T-G
MyVariant Identifiers: chr13:g.79380816T>G (hg19) chr13:g.78806681T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78806681T>G , CM000675.2:g.78806681T>G GRCh38
NC_000013.10:g.79380816T>G , CM000675.1:g.79380816T>G GRCh37
NC_000013.9:g.78278817T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046869.2:n.225-14379A>C
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