Canonical Allele Identifier: CA2639298424

Gene: SMARCD2

Linked Data

• gnomAD v4: 17-63832518-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832518A>G , CM000679.2:g.63832518A>G	GRCh38
NC_000017.10:g.61909878A>G , CM000679.1:g.61909878A>G	GRCh37
NC_000017.9:g.59263610A>G	NCBI36
NG_053004.1:g.15474T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2295T>C
ENST00000697953.1:n.2868T>C
ENST00000698013.1:n.2980T>C
ENST00000698014.1:n.3203T>C
ENST00000698015.1:n.2296T>C
ENST00000698016.1:c.*420T>C	ENSP00000513502.1:n.*420T>C
ENST00000698017.1:n.2370T>C
ENST00000698018.1:n.2501T>C
ENST00000698019.1:n.2699T>C
ENST00000698020.1:n.1805T>C
ENST00000698021.1:c.1714T>C
ENST00000698022.1:c.*420T>C	ENSP00000513504.1:n.*420T>C
ENST00000698023.1:n.2399T>C
ENST00000698024.1:n.2261T>C
ENST00000698025.1:n.2421T>C
ENST00000698026.1:n.1312T>C
ENST00000698027.1:c.*637T>C	ENSP00000513505.1:n.*637T>C
ENST00000698028.1:n.2504T>C
ENST00000698029.1:n.3233T>C
ENST00000448276.7:c.*420T>C MANE Select	ENSP00000392617.2:n.*420T>C
ENST00000323347.14:c.*420T>C	ENSP00000318451.10:n.*420T>C
ENST00000448276.6:c.*420T>C	ENSP00000392617.2:n.*420T>C
ENST00000613943.4:c.1905T>C	ENSP00000483605.1:n.1905T>C
NM_001098426.1:c.*420T>C	NP_001091896.1:n.*420T>C
XM_005257604.2:c.*420T>C	XP_005257661.2:n.*420T>C
NM_001330439.1:c.*420T>C	NP_001317368.1:n.*420T>C
NM_001330440.1:c.*420T>C	NP_001317369.1:n.*420T>C
NM_001098426.2:c.*420T>C MANE Select	NP_001091896.1:n.*420T>C
NM_001330440.2:c.*420T>C	NP_001317369.1:n.*420T>C