Canonical Allele Identifier: CA2494534970

Gene: SIX3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.44942875G= , CM000664.2:g.44942875G=	GRCh38
NC_000002.11:g.45170014G= , CM000664.1:g.45170014G=	GRCh37
NC_000002.10:g.45023518G=	NCBI36
NG_016222.1:g.5978G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260653.5:c.771G= MANE Select	ENSP00000260653.3:p.Arg257=
ENST00000260653.4:c.771G=	ENSP00000260653.3:p.Arg257=
NM_005413.3:c.771G=	NP_005404.1:p.Arg257=
XM_011533042.1:c.771G=	XP_011531344.1:p.Arg257=
NM_005413.4:c.771G= MANE Select	NP_005404.1:p.Arg257=