Canonical Allele Identifier: CA2270103022

Gene: SMARCD2

Linked Data

• dbSNP Id: rs2040198410
• gnomAD v4: 17-63832136-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832136C>T , CM000679.2:g.63832136C>T	GRCh38
NC_000017.10:g.61909496C>T , CM000679.1:g.61909496C>T	GRCh37
NC_000017.9:g.59263228C>T	NCBI36
NG_053004.1:g.15856G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000697953.1:n.3250G>A
ENST00000698013.1:n.3362G>A
ENST00000698014.1:n.3585G>A
ENST00000698015.1:n.2678G>A
ENST00000698016.1:c.*802G>A	ENSP00000513502.1:n.*802G>A
ENST00000698017.1:n.2752G>A
ENST00000698018.1:n.2883G>A
ENST00000698019.1:n.3081G>A
ENST00000698020.1:n.2187G>A
ENST00000698021.1:c.2096G>A
ENST00000698022.1:c.*802G>A	ENSP00000513504.1:n.*802G>A
ENST00000698023.1:n.2781G>A
ENST00000698024.1:n.2643G>A
ENST00000698025.1:n.2803G>A
ENST00000698026.1:n.1694G>A
ENST00000698027.1:c.*1019G>A	ENSP00000513505.1:n.*1019G>A
ENST00000448276.7:c.*802G>A MANE Select	ENSP00000392617.2:n.*802G>A
ENST00000448276.6:c.*802G>A	ENSP00000392617.2:n.*802G>A
ENST00000613943.4:c.2287G>A	ENSP00000483605.1:n.2287G>A
NM_001098426.1:c.*802G>A	NP_001091896.1:n.*802G>A
XM_005257604.2:c.*802G>A	XP_005257661.2:n.*802G>A
NM_001330439.1:c.*802G>A	NP_001317368.1:n.*802G>A
NM_001330440.1:c.*802G>A	NP_001317369.1:n.*802G>A
NM_001098426.2:c.*802G>A MANE Select	NP_001091896.1:n.*802G>A
NM_001330440.2:c.*802G>A	NP_001317369.1:n.*802G>A