Canonical Allele Identifier: CA1954821622
Gene: SOX6 HGNC NCBI
C11orf58 HGNC NCBI

Linked Data

dbSNP Id: rs1848384802

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.16735534C>T , CM000673.2:g.16735534C>T GRCh38
NC_000011.9:g.16757081C>T , CM000673.1:g.16757081C>T GRCh37
NC_000011.8:g.16713657C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000524520.5:n.353+805G>A (SOX6)
ENST00000525259.1:n.267+805G>A (SOX6)
ENST00000527893.5:n.405-9067C>T (C11orf58)
ENST00000530378.5:c.-335+805G>A (SOX6) ENSP00000432577.1:n.-335+805G>A
NM_001367872.1:c.-261+2891G>A (SOX6) NP_001354801.1:n.-261+2891G>A