Canonical Allele Identifier: CA2270107038
Gene: SMARCD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63840722A= , CM000679.2:g.63840722A= GRCh38
NC_000017.10:g.61918082A= , CM000679.1:g.61918082A= GRCh37
NC_000017.9:g.59271814A= NCBI36
NG_053004.1:g.7270T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697953.1:n.104+1737T=
ENST00000698022.1:c.33+1737T= ENSP00000513504.1:n.33+1737T=
ENST00000448276.7:c.216+1737T= MANE Select ENSP00000392617.2:n.216+1737T=
ENST00000225742.13:c.-10+1659T= ENSP00000225742.9:n.-10+1659T=
ENST00000448276.6:c.216+1737T= ENSP00000392617.2:n.216+1737T=
ENST00000577686.1:n.52+1737T=
ENST00000584400.5:c.216+1737T= ENSP00000464503.1:n.216+1737T=
ENST00000613943.4:c.105+1737T= ENSP00000483605.1:n.105+1737T=
NM_001098426.1:c.216+1737T= NP_001091896.1:n.216+1737T=
XM_005257604.2:c.-10+1659T= XP_005257661.2:n.-10+1659T=
NM_001330439.1:c.-10+1659T= NP_001317368.1:n.-10+1659T=
NM_001098426.2:c.216+1737T= MANE Select NP_001091896.1:n.216+1737T=