Canonical Allele Identifier: CA2639297990

Gene: SMARCD2

Linked Data

• gnomAD v4: 17-63832124-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832124A>T , CM000679.2:g.63832124A>T	GRCh38
NC_000017.10:g.61909484A>T , CM000679.1:g.61909484A>T	GRCh37
NC_000017.9:g.59263216A>T	NCBI36
NG_053004.1:g.15868T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.3262T>A
ENST00000698013.1:n.3374T>A
ENST00000698014.1:n.3597T>A
ENST00000698015.1:n.2690T>A
ENST00000698016.1:c.*814T>A	ENSP00000513502.1:n.*814T>A
ENST00000698017.1:n.2764T>A
ENST00000698018.1:n.2895T>A
ENST00000698019.1:n.3093T>A
ENST00000698020.1:n.2199T>A
ENST00000698021.1:c.2108T>A
ENST00000698022.1:c.*814T>A	ENSP00000513504.1:n.*814T>A
ENST00000698023.1:n.2793T>A
ENST00000698024.1:n.2655T>A
ENST00000448276.7:c.*814T>A MANE Select	ENSP00000392617.2:n.*814T>A
ENST00000448276.6:c.*814T>A	ENSP00000392617.2:n.*814T>A
ENST00000613943.4:c.2299T>A	ENSP00000483605.1:n.2299T>A
NM_001098426.1:c.*814T>A	NP_001091896.1:n.*814T>A
XM_005257604.2:c.*814T>A	XP_005257661.2:n.*814T>A
NM_001330439.1:c.*814T>A	NP_001317368.1:n.*814T>A
NM_001330440.1:c.*814T>A	NP_001317369.1:n.*814T>A
NM_001098426.2:c.*814T>A MANE Select	NP_001091896.1:n.*814T>A
NM_001330440.2:c.*814T>A	NP_001317369.1:n.*814T>A