Canonical Allele Identifier: CA2038244191

Gene: SMARCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56163782G= , CM000674.2:g.56163782G=	GRCh38
NC_000012.11:g.56557566G= , CM000674.1:g.56557566G=	GRCh37
NC_000012.10:g.54843833G=	NCBI36
NG_047081.1:g.30786C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000550164.6:c.3662-17C= MANE Select	ENSP00000449396.1:n.3662-17C=
ENST00000267064.8:c.3569-17C=	ENSP00000267064.4:n.3569-17C=
ENST00000347471.8:c.3317-17C=	ENSP00000302919.4:n.3317-17C=
ENST00000394023.7:c.3383-17C=	ENSP00000377591.3:n.3383-17C=
ENST00000550164.5:c.3662-17C=	ENSP00000449396.1:n.3662-17C=
ENST00000552674.5:c.*2980-17C=	ENSP00000447680.1:n.*2980-17C=
NM_001130420.1:c.3383-17C=	NP_001123892.1:n.3383-17C=
NM_003075.3:c.3569-17C=	NP_003066.2:n.3569-17C=
NM_139067.2:c.3317-17C=	NP_620706.1:n.3317-17C=
XM_005269101.1:c.3662-17C=	XP_005269158.1:n.3662-17C=
XM_005269102.1:c.3659-17C=	XP_005269159.1:n.3659-17C=
XM_005269103.1:c.3566-17C=	XP_005269160.1:n.3566-17C=
XM_005269104.1:c.3380-17C=	XP_005269161.1:n.3380-17C=
XM_011538693.1:c.2909-17C=	XP_011536995.1:n.2909-17C=
NM_001130420.2:c.3383-17C=	NP_001123892.1:n.3383-17C=
NM_001330288.1:c.3662-17C=	NP_001317217.1:n.3662-17C=
NM_003075.4:c.3569-17C=	NP_003066.2:n.3569-17C=
NM_139067.3:c.3317-17C=	NP_620706.1:n.3317-17C=
XM_005269102.2:c.3659-17C=	XP_005269159.1:n.3659-17C=
XM_005269103.2:c.3566-17C=	XP_005269160.1:n.3566-17C=
XM_011538693.3:c.2909-17C=	XP_011536995.1:n.2909-17C=
XM_017019884.1:c.3314-17C=	XP_016875373.1:n.3314-17C=
XM_017019885.1:c.3290-17C=	XP_016875374.1:n.3290-17C=
XM_017019886.1:c.3224-17C=	XP_016875375.1:n.3224-17C=
XM_017019887.2:c.2816-17C=	XP_016875376.1:n.2816-17C=
XR_002957373.1:n.3446-17C=
XR_002957374.1:n.3167-17C=
NM_001330288.2:c.3662-17C= MANE Select	NP_001317217.1:n.3662-17C=
NM_001130420.3:c.3383-17C=	NP_001123892.1:n.3383-17C=
NM_003075.5:c.3569-17C=	NP_003066.2:n.3569-17C=
NM_139067.4:c.3317-17C=	NP_620706.1:n.3317-17C=