Canonical Allele Identifier: CA2494534867
Gene: SIX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44942130T= , CM000664.2:g.44942130T= GRCh38
NC_000002.11:g.45169269T= , CM000664.1:g.45169269T= GRCh37
NC_000002.10:g.45022773T= NCBI36
NG_016222.1:g.5233T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260653.5:c.26T= MANE Select ENSP00000260653.3:p.Leu9=
ENST00000260653.4:c.26T= ENSP00000260653.3:p.Leu9=
NM_005413.3:c.26T= NP_005404.1:p.Leu9=
XM_011533042.1:c.26T= XP_011531344.1:p.Leu9=
NM_005413.4:c.26T= MANE Select NP_005404.1:p.Leu9=