Canonical Allele Identifier: CA2728271716
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs2137296485

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836587A>G , CM000675.2:g.78836587A>G GRCh38
NC_000013.10:g.79410722A>G , CM000675.1:g.79410722A>G GRCh37
NC_000013.9:g.78308723A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046869.2:n.111+3353T>C