Canonical Allele Identifier: CA2270102991

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832088C= , CM000679.2:g.63832088C=	GRCh38
NC_000017.10:g.61909448C= , CM000679.1:g.61909448C=	GRCh37
NC_000017.9:g.59263180C=	NCBI36
NG_053004.1:g.15904G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448276.7:c.*850G= MANE Select	ENSP00000392617.2:n.*850G=
ENST00000448276.6:c.*850G=	ENSP00000392617.2:n.*850G=
ENST00000613943.4:c.2335G=	ENSP00000483605.1:n.2335G=
NM_001098426.1:c.*850G=	NP_001091896.1:n.*850G=
XM_005257604.2:c.*850G=	XP_005257661.2:n.*850G=
NM_001330439.1:c.*850G=	NP_001317368.1:n.*850G=
NM_001330440.1:c.*850G=	NP_001317369.1:n.*850G=
NM_001098426.2:c.*850G= MANE Select	NP_001091896.1:n.*850G=
NM_001330440.2:c.*850G=	NP_001317369.1:n.*850G=