Canonical Allele Identifier: CA2494534962

Gene: SIX3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.44942215T= , CM000664.2:g.44942215T=	GRCh38
NC_000002.11:g.45169354T= , CM000664.1:g.45169354T=	GRCh37
NC_000002.10:g.45022858T=	NCBI36
NG_016222.1:g.5318T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260653.5:c.111T= MANE Select	ENSP00000260653.3:p.Gly37=
ENST00000260653.4:c.111T=	ENSP00000260653.3:p.Gly37=
NM_005413.3:c.111T=	NP_005404.1:p.Gly37=
XM_011533042.1:c.111T=	XP_011531344.1:p.Gly37=
NM_005413.4:c.111T= MANE Select	NP_005404.1:p.Gly37=