Canonical Allele Identifier: CA253224642
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs11838918

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836439T>C , CM000675.2:g.78836439T>C GRCh38
NC_000013.10:g.79410574T>C , CM000675.1:g.79410574T>C GRCh37
NC_000013.9:g.78308575T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046869.2:n.111+3501A>G