Canonical Allele Identifier: CA2270107045

Gene: SMARCD2

Linked Data

• dbSNP Id: rs1904427201

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63840733C>T , CM000679.2:g.63840733C>T	GRCh38
NC_000017.10:g.61918093C>T , CM000679.1:g.61918093C>T	GRCh37
NC_000017.9:g.59271825C>T	NCBI36
NG_053004.1:g.7259G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.104+1726G>A
ENST00000698022.1:c.33+1726G>A	ENSP00000513504.1:n.33+1726G>A
ENST00000448276.7:c.216+1726G>A MANE Select	ENSP00000392617.2:n.216+1726G>A
ENST00000225742.13:c.-10+1648G>A	ENSP00000225742.9:n.-10+1648G>A
ENST00000448276.6:c.216+1726G>A	ENSP00000392617.2:n.216+1726G>A
ENST00000577686.1:n.52+1726G>A
ENST00000584400.5:c.216+1726G>A	ENSP00000464503.1:n.216+1726G>A
ENST00000613943.4:c.105+1726G>A	ENSP00000483605.1:n.105+1726G>A
NM_001098426.1:c.216+1726G>A	NP_001091896.1:n.216+1726G>A
XM_005257604.2:c.-10+1648G>A	XP_005257661.2:n.-10+1648G>A
NM_001330439.1:c.-10+1648G>A	NP_001317368.1:n.-10+1648G>A
NM_001098426.2:c.216+1726G>A MANE Select	NP_001091896.1:n.216+1726G>A