Canonical Allele Identifier: CA1554040997

Gene: SMN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70049642T= , CM000667.2:g.70049642T=	GRCh38
NC_000005.9:g.69345469T= , CM000667.1:g.69345469T=	GRCh37
NC_000005.8:g.69381225T=	NCBI36
NG_008728.1:g.5120T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000380743.8:c.-44T=	ENSP00000370119.4:n.-44T=
ENST00000511812.5:c.-44T=	ENSP00000424282.1:n.-44T=
NM_017411.3:c.-44T=	NP_059107.1:n.-44T=
NM_022875.2:c.-44T=	NP_075013.1:n.-44T=
NM_022876.2:c.-44T=	NP_075014.1:n.-44T=
NM_022877.2:c.-44T=	NP_075015.1:n.-44T=
XM_011543600.1:c.-44T=	XP_011541902.1:n.-44T=
XM_011543601.1:c.-44T=	XP_011541903.1:n.-44T=
XM_011543602.1:c.-44T=	XP_011541904.1:n.-44T=
XM_011543603.1:c.-44T=	XP_011541905.1:n.-44T=
XR_948432.1:n.1054+61638T=
XM_011543600.2:c.-44T=	XP_011541902.1:n.-44T=
XM_011543602.3:c.-44T=	XP_011541904.1:n.-44T=
XM_011543603.3:c.-44T=	XP_011541905.1:n.-44T=