Canonical Allele Identifier: CA1619098650
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1763437107

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306609C>G , CM000668.2:g.31306609C>G GRCh38
NC_000006.11:g.31274386C>G , CM000668.1:g.31274386C>G GRCh37
NC_000006.10:g.31382365C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+169G>C
XR_926691.2:n.965+169G>C