Canonical Allele Identifier: CA773992972

Gene: SMARCD2

Linked Data

• dbSNP Id: rs1243067379
• gnomAD v4: 17-63832178-A-G
• MyVariant Identifiers: chr17:g.61909538A>G (hg19) ; chr17:g.63832178A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832178A>G , CM000679.2:g.63832178A>G	GRCh38
NC_000017.10:g.61909538A>G , CM000679.1:g.61909538A>G	GRCh37
NC_000017.9:g.59263270A>G	NCBI36
NG_053004.1:g.15814T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2635T>C
ENST00000697953.1:n.3208T>C
ENST00000698013.1:n.3320T>C
ENST00000698014.1:n.3543T>C
ENST00000698015.1:n.2636T>C
ENST00000698016.1:c.*760T>C	ENSP00000513502.1:n.*760T>C
ENST00000698017.1:n.2710T>C
ENST00000698018.1:n.2841T>C
ENST00000698019.1:n.3039T>C
ENST00000698020.1:n.2145T>C
ENST00000698021.1:c.2054T>C
ENST00000698022.1:c.*760T>C	ENSP00000513504.1:n.*760T>C
ENST00000698023.1:n.2739T>C
ENST00000698024.1:n.2601T>C
ENST00000698025.1:n.2761T>C
ENST00000698026.1:n.1652T>C
ENST00000698027.1:c.*977T>C	ENSP00000513505.1:n.*977T>C
ENST00000448276.7:c.*760T>C MANE Select	ENSP00000392617.2:n.*760T>C
ENST00000448276.6:c.*760T>C	ENSP00000392617.2:n.*760T>C
ENST00000613943.4:c.2245T>C	ENSP00000483605.1:n.2245T>C
NM_001098426.1:c.*760T>C	NP_001091896.1:n.*760T>C
XM_005257604.2:c.*760T>C	XP_005257661.2:n.*760T>C
NM_001330439.1:c.*760T>C	NP_001317368.1:n.*760T>C
NM_001330440.1:c.*760T>C	NP_001317369.1:n.*760T>C
NM_001098426.2:c.*760T>C MANE Select	NP_001091896.1:n.*760T>C
NM_001330440.2:c.*760T>C	NP_001317369.1:n.*760T>C