Canonical Allele Identifier: CA2494535099
Gene: SIX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44942296C= , CM000664.2:g.44942296C= GRCh38
NC_000002.11:g.45169435C= , CM000664.1:g.45169435C= GRCh37
NC_000002.10:g.45022939C= NCBI36
NG_016222.1:g.5399C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260653.5:c.192C= MANE Select ENSP00000260653.3:p.Gly64=
ENST00000260653.4:c.192C= ENSP00000260653.3:p.Gly64=
NM_005413.3:c.192C= NP_005404.1:p.Gly64=
XM_011533042.1:c.192C= XP_011531344.1:p.Gly64=
NM_005413.4:c.192C= MANE Select NP_005404.1:p.Gly64=