Canonical Allele Identifier: CA2494534858

Gene: SIX3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.44942118C= , CM000664.2:g.44942118C=	GRCh38
NC_000002.11:g.45169257C= , CM000664.1:g.45169257C=	GRCh37
NC_000002.10:g.45022761C=	NCBI36
NG_016222.1:g.5221C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260653.5:c.14C= MANE Select	ENSP00000260653.3:p.Ser5=
ENST00000260653.4:c.14C=	ENSP00000260653.3:p.Ser5=
NM_005413.3:c.14C=	NP_005404.1:p.Ser5=
XM_011533042.1:c.14C=	XP_011531344.1:p.Ser5=
NM_005413.4:c.14C= MANE Select	NP_005404.1:p.Ser5=