Canonical Allele Identifier: CA2733861365

Gene: SMARCD2

Linked Data

• dbSNP Id: rs2144622760

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832333G>A , CM000679.2:g.63832333G>A	GRCh38
NC_000017.10:g.61909693G>A , CM000679.1:g.61909693G>A	GRCh37
NC_000017.9:g.59263425G>A	NCBI36
NG_053004.1:g.15659C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2480C>T
ENST00000697953.1:n.3053C>T
ENST00000698013.1:n.3165C>T
ENST00000698014.1:n.3388C>T
ENST00000698015.1:n.2481C>T
ENST00000698016.1:c.*605C>T	ENSP00000513502.1:n.*605C>T
ENST00000698017.1:n.2555C>T
ENST00000698018.1:n.2686C>T
ENST00000698019.1:n.2884C>T
ENST00000698020.1:n.1990C>T
ENST00000698021.1:c.1899C>T
ENST00000698022.1:c.*605C>T	ENSP00000513504.1:n.*605C>T
ENST00000698023.1:n.2584C>T
ENST00000698024.1:n.2446C>T
ENST00000698025.1:n.2606C>T
ENST00000698026.1:n.1497C>T
ENST00000698027.1:c.*822C>T	ENSP00000513505.1:n.*822C>T
ENST00000698028.1:n.2689C>T
ENST00000698029.1:n.3418C>T
ENST00000448276.7:c.*605C>T MANE Select	ENSP00000392617.2:n.*605C>T
ENST00000448276.6:c.*605C>T	ENSP00000392617.2:n.*605C>T
ENST00000613943.4:c.2090C>T	ENSP00000483605.1:n.2090C>T
NM_001098426.1:c.*605C>T	NP_001091896.1:n.*605C>T
XM_005257604.2:c.*605C>T	XP_005257661.2:n.*605C>T
NM_001330439.1:c.*605C>T	NP_001317368.1:n.*605C>T
NM_001330440.1:c.*605C>T	NP_001317369.1:n.*605C>T
NM_001098426.2:c.*605C>T MANE Select	NP_001091896.1:n.*605C>T
NM_001330440.2:c.*605C>T	NP_001317369.1:n.*605C>T