Canonical Allele Identifier: CA2494535150
Gene: SIX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44942320C= , CM000664.2:g.44942320C= GRCh38
NC_000002.11:g.45169459C= , CM000664.1:g.45169459C= GRCh37
NC_000002.10:g.45022963C= NCBI36
NG_016222.1:g.5423C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260653.5:c.216C= MANE Select ENSP00000260653.3:p.Ala72=
ENST00000260653.4:c.216C= ENSP00000260653.3:p.Ala72=
NM_005413.3:c.216C= NP_005404.1:p.Ala72=
XM_011533042.1:c.216C= XP_011531344.1:p.Ala72=
NM_005413.4:c.216C= MANE Select NP_005404.1:p.Ala72=