Canonical Allele Identifier: CA2270103020
Gene: SMARCD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63832134C= , CM000679.2:g.63832134C= GRCh38
NC_000017.10:g.61909494C= , CM000679.1:g.61909494C= GRCh37
NC_000017.9:g.59263226C= NCBI36
NG_053004.1:g.15858G=

Transcript Alleles

HGVS Amino-acid change
ENST00000697953.1:n.3252G=
ENST00000698013.1:n.3364G=
ENST00000698014.1:n.3587G=
ENST00000698015.1:n.2680G=
ENST00000698016.1:c.*804G= ENSP00000513502.1:n.*804G=
ENST00000698017.1:n.2754G=
ENST00000698018.1:n.2885G=
ENST00000698019.1:n.3083G=
ENST00000698020.1:n.2189G=
ENST00000698021.1:c.2098G=
ENST00000698022.1:c.*804G= ENSP00000513504.1:n.*804G=
ENST00000698023.1:n.2783G=
ENST00000698024.1:n.2645G=
ENST00000698025.1:n.2805G=
ENST00000698026.1:n.1696G=
ENST00000698027.1:c.*1021G= ENSP00000513505.1:n.*1021G=
ENST00000448276.7:c.*804G= MANE Select ENSP00000392617.2:n.*804G=
ENST00000448276.6:c.*804G= ENSP00000392617.2:n.*804G=
ENST00000613943.4:c.2289G= ENSP00000483605.1:n.2289G=
NM_001098426.1:c.*804G= NP_001091896.1:n.*804G=
XM_005257604.2:c.*804G= XP_005257661.2:n.*804G=
NM_001330439.1:c.*804G= NP_001317368.1:n.*804G=
NM_001330440.1:c.*804G= NP_001317369.1:n.*804G=
NM_001098426.2:c.*804G= MANE Select NP_001091896.1:n.*804G=
NM_001330440.2:c.*804G= NP_001317369.1:n.*804G=