Canonical Allele Identifier: CA2639297983

Gene: SMARCD2

Linked Data

• gnomAD v4: 17-63832119-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832119G>A , CM000679.2:g.63832119G>A	GRCh38
NC_000017.10:g.61909479G>A , CM000679.1:g.61909479G>A	GRCh37
NC_000017.9:g.59263211G>A	NCBI36
NG_053004.1:g.15873C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.3267C>T
ENST00000698013.1:n.3379C>T
ENST00000698014.1:n.3602C>T
ENST00000698015.1:n.2695C>T
ENST00000698016.1:c.*819C>T	ENSP00000513502.1:n.*819C>T
ENST00000698017.1:n.2769C>T
ENST00000698018.1:n.2900C>T
ENST00000698019.1:n.3098C>T
ENST00000698020.1:n.2204C>T
ENST00000698021.1:c.2113C>T
ENST00000698022.1:c.*819C>T	ENSP00000513504.1:n.*819C>T
ENST00000698023.1:n.2798C>T
ENST00000698024.1:n.2660C>T
ENST00000448276.7:c.*819C>T MANE Select	ENSP00000392617.2:n.*819C>T
ENST00000448276.6:c.*819C>T	ENSP00000392617.2:n.*819C>T
ENST00000613943.4:c.2304C>T	ENSP00000483605.1:n.2304C>T
NM_001098426.1:c.*819C>T	NP_001091896.1:n.*819C>T
XM_005257604.2:c.*819C>T	XP_005257661.2:n.*819C>T
NM_001330439.1:c.*819C>T	NP_001317368.1:n.*819C>T
NM_001330440.1:c.*819C>T	NP_001317369.1:n.*819C>T
NM_001098426.2:c.*819C>T MANE Select	NP_001091896.1:n.*819C>T
NM_001330440.2:c.*819C>T	NP_001317369.1:n.*819C>T