Canonical Allele Identifier: CA773993209

Gene: SMARCD2

Linked Data

• dbSNP Id: rs1269860553
• MyVariant Identifiers: chr17:g.61909849C>G (hg19) ; chr17:g.63832489C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832489C>G , CM000679.2:g.63832489C>G	GRCh38
NC_000017.10:g.61909849C>G , CM000679.1:g.61909849C>G	GRCh37
NC_000017.9:g.59263581C>G	NCBI36
NG_053004.1:g.15503G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2324G>C
ENST00000697953.1:n.2897G>C
ENST00000698013.1:n.3009G>C
ENST00000698014.1:n.3232G>C
ENST00000698015.1:n.2325G>C
ENST00000698016.1:c.*449G>C	ENSP00000513502.1:n.*449G>C
ENST00000698017.1:n.2399G>C
ENST00000698018.1:n.2530G>C
ENST00000698019.1:n.2728G>C
ENST00000698020.1:n.1834G>C
ENST00000698021.1:c.1743G>C
ENST00000698022.1:c.*449G>C	ENSP00000513504.1:n.*449G>C
ENST00000698023.1:n.2428G>C
ENST00000698024.1:n.2290G>C
ENST00000698025.1:n.2450G>C
ENST00000698026.1:n.1341G>C
ENST00000698027.1:c.*666G>C	ENSP00000513505.1:n.*666G>C
ENST00000698028.1:n.2533G>C
ENST00000698029.1:n.3262G>C
ENST00000448276.7:c.*449G>C MANE Select	ENSP00000392617.2:n.*449G>C
ENST00000448276.6:c.*449G>C	ENSP00000392617.2:n.*449G>C
ENST00000613943.4:c.1934G>C	ENSP00000483605.1:n.1934G>C
NM_001098426.1:c.*449G>C	NP_001091896.1:n.*449G>C
XM_005257604.2:c.*449G>C	XP_005257661.2:n.*449G>C
NM_001330439.1:c.*449G>C	NP_001317368.1:n.*449G>C
NM_001330440.1:c.*449G>C	NP_001317369.1:n.*449G>C
NM_001098426.2:c.*449G>C MANE Select	NP_001091896.1:n.*449G>C
NM_001330440.2:c.*449G>C	NP_001317369.1:n.*449G>C