Canonical Allele Identifier: CA2494534979

Gene: SIX3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.44942887C= , CM000664.2:g.44942887C=	GRCh38
NC_000002.11:g.45170026C= , CM000664.1:g.45170026C=	GRCh37
NC_000002.10:g.45023530C=	NCBI36
NG_016222.1:g.5990C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260653.5:c.783C= MANE Select	ENSP00000260653.3:p.Asp261=
ENST00000260653.4:c.783C=	ENSP00000260653.3:p.Asp261=
NM_005413.3:c.783C=	NP_005404.1:p.Asp261=
XM_011533042.1:c.783C=	XP_011531344.1:p.Asp261=
NM_005413.4:c.783C= MANE Select	NP_005404.1:p.Asp261=