Canonical Allele Identifier: CA701182661

Gene: LINC00331

Linked Data

• dbSNP Id: rs1275727742
• gnomAD v3: 13-78836407-T-C
• gnomAD v4: 13-78836407-T-C
• MyVariant Identifiers: chr13:g.79410542T>C (hg19) ; chr13:g.78836407T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.78836407T>C , CM000675.2:g.78836407T>C	GRCh38
NC_000013.10:g.79410542T>C , CM000675.1:g.79410542T>C	GRCh37
NC_000013.9:g.78308543T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046869.2:n.111+3533A>G