Canonical Allele Identifier: CA2639298057

Gene: SMARCD2

Linked Data

• gnomAD v4: 17-63832163-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832163A>G , CM000679.2:g.63832163A>G	GRCh38
NC_000017.10:g.61909523A>G , CM000679.1:g.61909523A>G	GRCh37
NC_000017.9:g.59263255A>G	NCBI36
NG_053004.1:g.15829T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2650T>C
ENST00000697953.1:n.3223T>C
ENST00000698013.1:n.3335T>C
ENST00000698014.1:n.3558T>C
ENST00000698015.1:n.2651T>C
ENST00000698016.1:c.*775T>C	ENSP00000513502.1:n.*775T>C
ENST00000698017.1:n.2725T>C
ENST00000698018.1:n.2856T>C
ENST00000698019.1:n.3054T>C
ENST00000698020.1:n.2160T>C
ENST00000698021.1:c.2069T>C
ENST00000698022.1:c.*775T>C	ENSP00000513504.1:n.*775T>C
ENST00000698023.1:n.2754T>C
ENST00000698024.1:n.2616T>C
ENST00000698025.1:n.2776T>C
ENST00000698026.1:n.1667T>C
ENST00000698027.1:c.*992T>C	ENSP00000513505.1:n.*992T>C
ENST00000448276.7:c.*775T>C MANE Select	ENSP00000392617.2:n.*775T>C
ENST00000448276.6:c.*775T>C	ENSP00000392617.2:n.*775T>C
ENST00000613943.4:c.2260T>C	ENSP00000483605.1:n.2260T>C
NM_001098426.1:c.*775T>C	NP_001091896.1:n.*775T>C
XM_005257604.2:c.*775T>C	XP_005257661.2:n.*775T>C
NM_001330439.1:c.*775T>C	NP_001317368.1:n.*775T>C
NM_001330440.1:c.*775T>C	NP_001317369.1:n.*775T>C
NM_001098426.2:c.*775T>C MANE Select	NP_001091896.1:n.*775T>C
NM_001330440.2:c.*775T>C	NP_001317369.1:n.*775T>C