Canonical Allele Identifier: CA1619089567
Gene: LINC02571 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31295974T= , CM000668.2:g.31295974T= GRCh38
NC_000006.11:g.31263751T= , CM000668.1:g.31263751T= GRCh37
NC_000006.10:g.31371730T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_149115.1:n.167-961A=