Canonical Allele Identifier: CA2162093
Gene: LINC00471 HGNC NCBI

Linked Data

dbSNP Id: rs6750795

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.231513520T>C , CM000664.2:g.231513520T>C GRCh38
NC_000002.11:g.232378231T>C , CM000664.1:g.232378231T>C GRCh37
NC_000002.10:g.232086475T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024079.1:n.364+7A>G