Canonical Allele Identifier: CA2270107043
Gene: SMARCD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63840729T= , CM000679.2:g.63840729T= GRCh38
NC_000017.10:g.61918089T= , CM000679.1:g.61918089T= GRCh37
NC_000017.9:g.59271821T= NCBI36
NG_053004.1:g.7263A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697953.1:n.104+1730A=
ENST00000698022.1:c.33+1730A= ENSP00000513504.1:n.33+1730A=
ENST00000448276.7:c.216+1730A= MANE Select ENSP00000392617.2:n.216+1730A=
ENST00000225742.13:c.-10+1652A= ENSP00000225742.9:n.-10+1652A=
ENST00000448276.6:c.216+1730A= ENSP00000392617.2:n.216+1730A=
ENST00000577686.1:n.52+1730A=
ENST00000584400.5:c.216+1730A= ENSP00000464503.1:n.216+1730A=
ENST00000613943.4:c.105+1730A= ENSP00000483605.1:n.105+1730A=
NM_001098426.1:c.216+1730A= NP_001091896.1:n.216+1730A=
XM_005257604.2:c.-10+1652A= XP_005257661.2:n.-10+1652A=
NM_001330439.1:c.-10+1652A= NP_001317368.1:n.-10+1652A=
NM_001098426.2:c.216+1730A= MANE Select NP_001091896.1:n.216+1730A=