Canonical Allele Identifier: CA2375128621

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.64049234A= , CM000682.2:g.64049234A= GRCh38
NC_000020.10:g.62680587A= , CM000682.1:g.62680587A= GRCh37
NC_000020.9:g.62151031A= NCBI36
NG_008095.1:g.5393T=

Transcript Alleles

HGVS Amino-acid change
ENST00000340356.9:c.283T= (SOX18) MANE Select ENSP00000341815.7:p.Trp95=
ENST00000340356.8:c.283T= (SOX18) ENSP00000341815.7:p.Trp95=
NM_018419.2:c.283T= (SOX18) NP_060889.1:p.Trp95=
XM_011529022.1:c.-2320+6839A= (TCEA2) XP_011527324.1:n.-2320+6839A=
XM_011529025.1:c.-2236+6839A= (TCEA2) XP_011527327.1:n.-2236+6839A=
XM_024451978.1:c.-2236+6839A= (TCEA2) XP_024307746.1:n.-2236+6839A=
NM_018419.3:c.283T= (SOX18) MANE Select NP_060889.1:p.Trp95=