Canonical Allele Identifier: CA2639298097

Gene: SMARCD2

Linked Data

• gnomAD v4: 17-63832193-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832193G>A , CM000679.2:g.63832193G>A	GRCh38
NC_000017.10:g.61909553G>A , CM000679.1:g.61909553G>A	GRCh37
NC_000017.9:g.59263285G>A	NCBI36
NG_053004.1:g.15799C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2620C>T
ENST00000697953.1:n.3193C>T
ENST00000698013.1:n.3305C>T
ENST00000698014.1:n.3528C>T
ENST00000698015.1:n.2621C>T
ENST00000698016.1:c.*745C>T	ENSP00000513502.1:n.*745C>T
ENST00000698017.1:n.2695C>T
ENST00000698018.1:n.2826C>T
ENST00000698019.1:n.3024C>T
ENST00000698020.1:n.2130C>T
ENST00000698021.1:c.2039C>T
ENST00000698022.1:c.*745C>T	ENSP00000513504.1:n.*745C>T
ENST00000698023.1:n.2724C>T
ENST00000698024.1:n.2586C>T
ENST00000698025.1:n.2746C>T
ENST00000698026.1:n.1637C>T
ENST00000698027.1:c.*962C>T	ENSP00000513505.1:n.*962C>T
ENST00000698028.1:n.2829C>T
ENST00000448276.7:c.*745C>T MANE Select	ENSP00000392617.2:n.*745C>T
ENST00000448276.6:c.*745C>T	ENSP00000392617.2:n.*745C>T
ENST00000613943.4:c.2230C>T	ENSP00000483605.1:n.2230C>T
NM_001098426.1:c.*745C>T	NP_001091896.1:n.*745C>T
XM_005257604.2:c.*745C>T	XP_005257661.2:n.*745C>T
NM_001330439.1:c.*745C>T	NP_001317368.1:n.*745C>T
NM_001330440.1:c.*745C>T	NP_001317369.1:n.*745C>T
NM_001098426.2:c.*745C>T MANE Select	NP_001091896.1:n.*745C>T
NM_001330440.2:c.*745C>T	NP_001317369.1:n.*745C>T