Canonical Allele Identifier: CA823866987
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1427890152
MyVariant Identifiers: chr6:g.31274180A>C (hg19) chr6:g.31306403A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306403A>C , CM000668.2:g.31306403A>C GRCh38
NC_000006.11:g.31274180A>C , CM000668.1:g.31274180A>C GRCh37
NC_000006.10:g.31382159A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926691.1:n.949+375T>G
XR_926691.2:n.965+375T>G
Search 100 bp 5'
Search 100 bp 3'