Canonical Allele Identifier: CA31223048

Gene: LINC02819

Linked Data

• dbSNP Id: rs909744331
• MyVariant Identifiers: chr1:g.159453866T>C (hg19) ; chr1:g.159484076T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159484076T>C , CM000663.2:g.159484076T>C	GRCh38
NC_000001.10:g.159453866T>C , CM000663.1:g.159453866T>C	GRCh37
NC_000001.9:g.157720490T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922189.1:n.678+1092T>C
XR_922189.3:n.690+1092T>C