Canonical Allele Identifier: CA2639298400

Gene: SMARCD2

Linked Data

• gnomAD v4: 17-63832496-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832496G>T , CM000679.2:g.63832496G>T	GRCh38
NC_000017.10:g.61909856G>T , CM000679.1:g.61909856G>T	GRCh37
NC_000017.9:g.59263588G>T	NCBI36
NG_053004.1:g.15496C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2317C>A
ENST00000697953.1:n.2890C>A
ENST00000698013.1:n.3002C>A
ENST00000698014.1:n.3225C>A
ENST00000698015.1:n.2318C>A
ENST00000698016.1:c.*442C>A	ENSP00000513502.1:n.*442C>A
ENST00000698017.1:n.2392C>A
ENST00000698018.1:n.2523C>A
ENST00000698019.1:n.2721C>A
ENST00000698020.1:n.1827C>A
ENST00000698021.1:c.1736C>A
ENST00000698022.1:c.*442C>A	ENSP00000513504.1:n.*442C>A
ENST00000698023.1:n.2421C>A
ENST00000698024.1:n.2283C>A
ENST00000698025.1:n.2443C>A
ENST00000698026.1:n.1334C>A
ENST00000698027.1:c.*659C>A	ENSP00000513505.1:n.*659C>A
ENST00000698028.1:n.2526C>A
ENST00000698029.1:n.3255C>A
ENST00000448276.7:c.*442C>A MANE Select	ENSP00000392617.2:n.*442C>A
ENST00000448276.6:c.*442C>A	ENSP00000392617.2:n.*442C>A
ENST00000613943.4:c.1927C>A	ENSP00000483605.1:n.1927C>A
NM_001098426.1:c.*442C>A	NP_001091896.1:n.*442C>A
XM_005257604.2:c.*442C>A	XP_005257661.2:n.*442C>A
NM_001330439.1:c.*442C>A	NP_001317368.1:n.*442C>A
NM_001330440.1:c.*442C>A	NP_001317369.1:n.*442C>A
NM_001098426.2:c.*442C>A MANE Select	NP_001091896.1:n.*442C>A
NM_001330440.2:c.*442C>A	NP_001317369.1:n.*442C>A