Canonical Allele Identifier: CA14383607
Gene: SMARCD2 HGNC NCBI

Linked Data

dbSNP Id: rs6919

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63832125T>A , CM000679.2:g.63832125T>A GRCh38
NC_000017.10:g.61909485T>A , CM000679.1:g.61909485T>A GRCh37
NC_000017.9:g.59263217T>A NCBI36
NG_053004.1:g.15867A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000697953.1:n.3261A>T
ENST00000698013.1:n.3373A>T
ENST00000698014.1:n.3596A>T
ENST00000698015.1:n.2689A>T
ENST00000698016.1:c.*813A>T ENSP00000513502.1:n.*813A>T
ENST00000698017.1:n.2763A>T
ENST00000698018.1:n.2894A>T
ENST00000698019.1:n.3092A>T
ENST00000698020.1:n.2198A>T
ENST00000698021.1:c.2107A>T
ENST00000698022.1:c.*813A>T ENSP00000513504.1:n.*813A>T
ENST00000698023.1:n.2792A>T
ENST00000698024.1:n.2654A>T
ENST00000448276.7:c.*813A>T MANE Select ENSP00000392617.2:n.*813A>T
ENST00000448276.6:c.*813A>T ENSP00000392617.2:n.*813A>T
ENST00000613943.4:c.2298A>T ENSP00000483605.1:n.2298A>T
NM_001098426.1:c.*813A>T NP_001091896.1:n.*813A>T
XM_005257604.2:c.*813A>T XP_005257661.2:n.*813A>T
NM_001330439.1:c.*813A>T NP_001317368.1:n.*813A>T
NM_001330440.1:c.*813A>T NP_001317369.1:n.*813A>T
NM_001098426.2:c.*813A>T MANE Select NP_001091896.1:n.*813A>T
NM_001330440.2:c.*813A>T NP_001317369.1:n.*813A>T