Canonical Allele Identifier: CA12187488
Gene: LINC02571 HGNC NCBI
dbSNP:
10484554
gnomAD v2:
6:31274555 C / T
gnomAD v3:
6:31306778 C / T
gnomAD v4:
chr6-31306778-C-T
Joint Max Group AF 0.1884514 (MID)
Genomes Max Group AF 0.15465739 (SAS)
MyVariant.info:
GRCh38 chr6:g.31306778C>T
GRCh37 chr6:g.31274555C>T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306778C>T , CM000668.2:g.31306778C>T GRCh38
NC_000006.11:g.31274555C>T , CM000668.1:g.31274555C>T GRCh37
NC_000006.10:g.31382534C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926691.1:n.949G>A
XR_926691.2:n.965G>A
Search 100 bp 5'
Search 100 bp 3'