Canonical Allele Identifier: CA773993169

Gene: SMARCD2

Linked Data

• dbSNP Id: rs1408628744
• gnomAD v3: 17-63832409-G-A
• gnomAD v4: 17-63832409-G-A
• MyVariant Identifiers: chr17:g.61909769G>A (hg19) ; chr17:g.63832409G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832409G>A , CM000679.2:g.63832409G>A	GRCh38
NC_000017.10:g.61909769G>A , CM000679.1:g.61909769G>A	GRCh37
NC_000017.9:g.59263501G>A	NCBI36
NG_053004.1:g.15583C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2404C>T
ENST00000697953.1:n.2977C>T
ENST00000698013.1:n.3089C>T
ENST00000698014.1:n.3312C>T
ENST00000698015.1:n.2405C>T
ENST00000698016.1:c.*529C>T	ENSP00000513502.1:n.*529C>T
ENST00000698017.1:n.2479C>T
ENST00000698018.1:n.2610C>T
ENST00000698019.1:n.2808C>T
ENST00000698020.1:n.1914C>T
ENST00000698021.1:c.1823C>T
ENST00000698022.1:c.*529C>T	ENSP00000513504.1:n.*529C>T
ENST00000698023.1:n.2508C>T
ENST00000698024.1:n.2370C>T
ENST00000698025.1:n.2530C>T
ENST00000698026.1:n.1421C>T
ENST00000698027.1:c.*746C>T	ENSP00000513505.1:n.*746C>T
ENST00000698028.1:n.2613C>T
ENST00000698029.1:n.3342C>T
ENST00000448276.7:c.*529C>T MANE Select	ENSP00000392617.2:n.*529C>T
ENST00000448276.6:c.*529C>T	ENSP00000392617.2:n.*529C>T
ENST00000613943.4:c.2014C>T	ENSP00000483605.1:n.2014C>T
NM_001098426.1:c.*529C>T	NP_001091896.1:n.*529C>T
XM_005257604.2:c.*529C>T	XP_005257661.2:n.*529C>T
NM_001330439.1:c.*529C>T	NP_001317368.1:n.*529C>T
NM_001330440.1:c.*529C>T	NP_001317369.1:n.*529C>T
NM_001098426.2:c.*529C>T MANE Select	NP_001091896.1:n.*529C>T
NM_001330440.2:c.*529C>T	NP_001317369.1:n.*529C>T