Canonical Allele Identifier: CA2639297953

Gene: SMARCD2

Linked Data

• gnomAD v4: 17-63832081-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832081C>A , CM000679.2:g.63832081C>A	GRCh38
NC_000017.10:g.61909441C>A , CM000679.1:g.61909441C>A	GRCh37
NC_000017.9:g.59263173C>A	NCBI36
NG_053004.1:g.15911G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448276.7:c.*857G>T MANE Select	ENSP00000392617.2:n.*857G>T
ENST00000613943.4:c.2342G>T	ENSP00000483605.1:n.2342G>T
NM_001098426.1:c.*857G>T	NP_001091896.1:n.*857G>T
XM_005257604.2:c.*857G>T	XP_005257661.2:n.*857G>T
NM_001330439.1:c.*857G>T	NP_001317368.1:n.*857G>T
NM_001330440.1:c.*857G>T	NP_001317369.1:n.*857G>T
NM_001098426.2:c.*857G>T MANE Select	NP_001091896.1:n.*857G>T
NM_001330440.2:c.*857G>T	NP_001317369.1:n.*857G>T