Canonical Allele Identifier: CA1235671389
Gene: SOX11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.5692883C= , CM000664.2:g.5692883C= GRCh38
NC_000002.11:g.5833015C= , CM000664.1:g.5833015C= GRCh37
NC_000002.10:g.5750466C= NCBI36
NG_050751.1:g.5217C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322002.5:c.162C= MANE Select ENSP00000322568.3:p.Asn54=
ENST00000322002.4:c.162C= ENSP00000322568.3:p.Asn54=
NM_003108.3:c.162C= NP_003099.1:p.Asn54=
NM_003108.4:c.162C= MANE Select NP_003099.1:p.Asn54=
Search 100 bp 5'
Search 100 bp 3'