Canonical Allele Identifier: CA1954821549
Gene: SOX6 HGNC NCBI
C11orf58 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.16735344G= , CM000673.2:g.16735344G= GRCh38
NC_000011.9:g.16756891G= , CM000673.1:g.16756891G= GRCh37
NC_000011.8:g.16713467G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000524520.5:n.353+995C= (SOX6)
ENST00000525259.1:n.267+995C= (SOX6)
ENST00000527893.5:n.405-9257G= (C11orf58)
ENST00000530378.5:c.-335+995C= (SOX6) ENSP00000432577.1:n.-335+995C=
NM_001367872.1:c.-261+3081C= (SOX6) NP_001354801.1:n.-261+3081C=