Canonical Allele Identifier: CA2038244183

Gene: SMARCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56163764G= , CM000674.2:g.56163764G=	GRCh38
NC_000012.11:g.56557548G= , CM000674.1:g.56557548G=	GRCh37
NC_000012.10:g.54843815G=	NCBI36
NG_047081.1:g.30804C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000550164.6:c.3663C= MANE Select	ENSP00000449396.1:p.Asp1221=
ENST00000267064.8:c.3570C=	ENSP00000267064.4:p.Asp1190=
ENST00000347471.8:c.3318C=	ENSP00000302919.4:p.Asp1106=
ENST00000394023.7:c.3384C=	ENSP00000377591.3:p.Asp1128=
ENST00000550164.5:c.3663C=	ENSP00000449396.1:p.Asp1221=
ENST00000552674.5:c.*2981C=	ENSP00000447680.1:n.*2981C=
NM_001130420.1:c.3384C=	NP_001123892.1:p.Asp1128=
NM_003075.3:c.3570C=	NP_003066.2:p.Asp1190=
NM_139067.2:c.3318C=	NP_620706.1:p.Asp1106=
XM_005269101.1:c.3663C=	XP_005269158.1:p.Asp1221=
XM_005269102.1:c.3660C=	XP_005269159.1:p.Asp1220=
XM_005269103.1:c.3567C=	XP_005269160.1:p.Asp1189=
XM_005269104.1:c.3381C=	XP_005269161.1:p.Asp1127=
XM_011538693.1:c.2910C=	XP_011536995.1:p.Asp970=
NM_001130420.2:c.3384C=	NP_001123892.1:p.Asp1128=
NM_001330288.1:c.3663C=	NP_001317217.1:p.Asp1221=
NM_003075.4:c.3570C=	NP_003066.2:p.Asp1190=
NM_139067.3:c.3318C=	NP_620706.1:p.Asp1106=
XM_005269102.2:c.3660C=	XP_005269159.1:p.Asp1220=
XM_005269103.2:c.3567C=	XP_005269160.1:p.Asp1189=
XM_011538693.3:c.2910C=	XP_011536995.1:p.Asp970=
XM_017019884.1:c.3315C=	XP_016875373.1:p.Asp1105=
XM_017019885.1:c.3291C=	XP_016875374.1:p.Asp1097=
XM_017019886.1:c.3225C=	XP_016875375.1:p.Asp1075=
XM_017019887.2:c.2817C=	XP_016875376.1:p.Asp939=
XR_002957373.1:n.3447C=
XR_002957374.1:n.3168C=
NM_001330288.2:c.3663C= MANE Select	NP_001317217.1:p.Asp1221=
NM_001130420.3:c.3384C=	NP_001123892.1:p.Asp1128=
NM_003075.5:c.3570C=	NP_003066.2:p.Asp1190=
NM_139067.4:c.3318C=	NP_620706.1:p.Asp1106=