Canonical Allele Identifier: CA254038891

Gene: LINC00333

Linked Data

• dbSNP Id: rs890450434
• gnomAD v2: 13-85032220-A-C
• gnomAD v3: 13-84458085-A-C
• gnomAD v4: 13-84458085-A-C
• MyVariant Identifiers: chr13:g.85032220A>C (hg19) ; chr13:g.84458085A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.84458085A>C , CM000675.2:g.84458085A>C	GRCh38
NC_000013.10:g.85032220A>C , CM000675.1:g.85032220A>C	GRCh37
NC_000013.9:g.83930221A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046871.1:n.139-104279A>C
XR_942133.1:n.369-46166T>G
XR_942134.1:n.366-46166T>G