Canonical Allele Identifier: CA2639298238

Gene: SMARCD2

Linked Data

• gnomAD v4: 17-63832319-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832319G>A , CM000679.2:g.63832319G>A	GRCh38
NC_000017.10:g.61909679G>A , CM000679.1:g.61909679G>A	GRCh37
NC_000017.9:g.59263411G>A	NCBI36
NG_053004.1:g.15673C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2494C>T
ENST00000697953.1:n.3067C>T
ENST00000698013.1:n.3179C>T
ENST00000698014.1:n.3402C>T
ENST00000698015.1:n.2495C>T
ENST00000698016.1:c.*619C>T	ENSP00000513502.1:n.*619C>T
ENST00000698017.1:n.2569C>T
ENST00000698018.1:n.2700C>T
ENST00000698019.1:n.2898C>T
ENST00000698020.1:n.2004C>T
ENST00000698021.1:c.1913C>T
ENST00000698022.1:c.*619C>T	ENSP00000513504.1:n.*619C>T
ENST00000698023.1:n.2598C>T
ENST00000698024.1:n.2460C>T
ENST00000698025.1:n.2620C>T
ENST00000698026.1:n.1511C>T
ENST00000698027.1:c.*836C>T	ENSP00000513505.1:n.*836C>T
ENST00000698028.1:n.2703C>T
ENST00000698029.1:n.3432C>T
ENST00000448276.7:c.*619C>T MANE Select	ENSP00000392617.2:n.*619C>T
ENST00000448276.6:c.*619C>T	ENSP00000392617.2:n.*619C>T
ENST00000613943.4:c.2104C>T	ENSP00000483605.1:n.2104C>T
NM_001098426.1:c.*619C>T	NP_001091896.1:n.*619C>T
XM_005257604.2:c.*619C>T	XP_005257661.2:n.*619C>T
NM_001330439.1:c.*619C>T	NP_001317368.1:n.*619C>T
NM_001330440.1:c.*619C>T	NP_001317369.1:n.*619C>T
NM_001098426.2:c.*619C>T MANE Select	NP_001091896.1:n.*619C>T
NM_001330440.2:c.*619C>T	NP_001317369.1:n.*619C>T