Canonical Allele Identifier: CA2639297976

Gene: SMARCD2

Linked Data

• gnomAD v4: 17-63832115-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832115A>T , CM000679.2:g.63832115A>T	GRCh38
NC_000017.10:g.61909475A>T , CM000679.1:g.61909475A>T	GRCh37
NC_000017.9:g.59263207A>T	NCBI36
NG_053004.1:g.15877T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.3271T>A
ENST00000698013.1:n.3383T>A
ENST00000698014.1:n.3606T>A
ENST00000698015.1:n.2699T>A
ENST00000698016.1:c.*823T>A	ENSP00000513502.1:n.*823T>A
ENST00000698017.1:n.2773T>A
ENST00000698018.1:n.2904T>A
ENST00000698019.1:n.3102T>A
ENST00000698020.1:n.2208T>A
ENST00000698021.1:c.2117T>A
ENST00000698022.1:c.*823T>A	ENSP00000513504.1:n.*823T>A
ENST00000698023.1:n.2802T>A
ENST00000698024.1:n.2664T>A
ENST00000448276.7:c.*823T>A MANE Select	ENSP00000392617.2:n.*823T>A
ENST00000448276.6:c.*823T>A	ENSP00000392617.2:n.*823T>A
ENST00000613943.4:c.2308T>A	ENSP00000483605.1:n.2308T>A
NM_001098426.1:c.*823T>A	NP_001091896.1:n.*823T>A
XM_005257604.2:c.*823T>A	XP_005257661.2:n.*823T>A
NM_001330439.1:c.*823T>A	NP_001317368.1:n.*823T>A
NM_001330440.1:c.*823T>A	NP_001317369.1:n.*823T>A
NM_001098426.2:c.*823T>A MANE Select	NP_001091896.1:n.*823T>A
NM_001330440.2:c.*823T>A	NP_001317369.1:n.*823T>A