Canonical Allele Identifier: CA292951568

Gene: SMARCD2

Linked Data

• dbSNP Id: rs970798892
• MyVariant Identifiers: chr17:g.61909540A>G (hg19) ; chr17:g.63832180A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832180A>G , CM000679.2:g.63832180A>G	GRCh38
NC_000017.10:g.61909540A>G , CM000679.1:g.61909540A>G	GRCh37
NC_000017.9:g.59263272A>G	NCBI36
NG_053004.1:g.15812T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2633T>C
ENST00000697953.1:n.3206T>C
ENST00000698013.1:n.3318T>C
ENST00000698014.1:n.3541T>C
ENST00000698015.1:n.2634T>C
ENST00000698016.1:c.*758T>C	ENSP00000513502.1:n.*758T>C
ENST00000698017.1:n.2708T>C
ENST00000698018.1:n.2839T>C
ENST00000698019.1:n.3037T>C
ENST00000698020.1:n.2143T>C
ENST00000698021.1:c.2052T>C
ENST00000698022.1:c.*758T>C	ENSP00000513504.1:n.*758T>C
ENST00000698023.1:n.2737T>C
ENST00000698024.1:n.2599T>C
ENST00000698025.1:n.2759T>C
ENST00000698026.1:n.1650T>C
ENST00000698027.1:c.*975T>C	ENSP00000513505.1:n.*975T>C
ENST00000448276.7:c.*758T>C MANE Select	ENSP00000392617.2:n.*758T>C
ENST00000448276.6:c.*758T>C	ENSP00000392617.2:n.*758T>C
ENST00000613943.4:c.2243T>C	ENSP00000483605.1:n.2243T>C
NM_001098426.1:c.*758T>C	NP_001091896.1:n.*758T>C
XM_005257604.2:c.*758T>C	XP_005257661.2:n.*758T>C
NM_001330439.1:c.*758T>C	NP_001317368.1:n.*758T>C
NM_001330440.1:c.*758T>C	NP_001317369.1:n.*758T>C
NM_001098426.2:c.*758T>C MANE Select	NP_001091896.1:n.*758T>C
NM_001330440.2:c.*758T>C	NP_001317369.1:n.*758T>C