Canonical Allele Identifier: CA2270103021
Gene: SMARCD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63832135G= , CM000679.2:g.63832135G= GRCh38
NC_000017.10:g.61909495G= , CM000679.1:g.61909495G= GRCh37
NC_000017.9:g.59263227G= NCBI36
NG_053004.1:g.15857C=

Transcript Alleles

HGVS Amino-acid change
ENST00000697953.1:n.3251C=
ENST00000698013.1:n.3363C=
ENST00000698014.1:n.3586C=
ENST00000698015.1:n.2679C=
ENST00000698016.1:c.*803C= ENSP00000513502.1:n.*803C=
ENST00000698017.1:n.2753C=
ENST00000698018.1:n.2884C=
ENST00000698019.1:n.3082C=
ENST00000698020.1:n.2188C=
ENST00000698021.1:c.2097C=
ENST00000698022.1:c.*803C= ENSP00000513504.1:n.*803C=
ENST00000698023.1:n.2782C=
ENST00000698024.1:n.2644C=
ENST00000698025.1:n.2804C=
ENST00000698026.1:n.1695C=
ENST00000698027.1:c.*1020C= ENSP00000513505.1:n.*1020C=
ENST00000448276.7:c.*803C= MANE Select ENSP00000392617.2:n.*803C=
ENST00000448276.6:c.*803C= ENSP00000392617.2:n.*803C=
ENST00000613943.4:c.2288C= ENSP00000483605.1:n.2288C=
NM_001098426.1:c.*803C= NP_001091896.1:n.*803C=
XM_005257604.2:c.*803C= XP_005257661.2:n.*803C=
NM_001330439.1:c.*803C= NP_001317368.1:n.*803C=
NM_001330440.1:c.*803C= NP_001317369.1:n.*803C=
NM_001098426.2:c.*803C= MANE Select NP_001091896.1:n.*803C=
NM_001330440.2:c.*803C= NP_001317369.1:n.*803C=