Canonical Allele Identifier: CA31223097

Gene: LINC02819

Linked Data

• dbSNP Id: rs976150119
• MyVariant Identifiers: chr1:g.159453985C>T (hg19) ; chr1:g.159484195C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159484195C>T , CM000663.2:g.159484195C>T	GRCh38
NC_000001.10:g.159453985C>T , CM000663.1:g.159453985C>T	GRCh37
NC_000001.9:g.157720609C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922189.1:n.678+1211C>T
XR_922189.3:n.690+1211C>T