Canonical Allele Identifier: CA8870666

Gene: SMCHD1

Linked Data

• ClinVar Variation Id: 284808
• ClinVar RCV Id: RCV000306911 ; RCV001407288
• dbSNP Id: rs145233420
• ExAC: 18:2694636 C / A
• gnomAD v2: 18-2694636-C-A
• gnomAD v3: 18-2694638-C-A
• gnomAD v4: 18-2694638-C-A
• MyVariant Identifiers: chr18:g.2694636C>A (hg19) ; chr18:g.2694638C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2694638C>A , CM000680.2:g.2694638C>A	GRCh38
NC_000018.9:g.2694636C>A , CM000680.1:g.2694636C>A	GRCh37
NC_000018.8:g.2684636C>A	NCBI36
NG_031972.1:g.43751C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684915.1:n.1142C>A
ENST00000688342.1:c.985C>A	ENSP00000508422.1:p.Pro329Thr
ENST00000693213.1:n.263C>A
ENST00000320876.11:c.985C>A MANE Select	ENSP00000326603.7:p.Pro329Thr
ENST00000320876.10:c.985C>A	ENSP00000326603.6:p.Pro329Thr
ENST00000581226.1:n.219C>A
NM_015295.2:c.985C>A	NP_056110.2:p.Pro329Thr
XM_011525642.1:c.985C>A	XP_011523944.1:p.Pro329Thr
XM_011525643.1:c.985C>A	XP_011523945.1:p.Pro329Thr
XM_011525644.1:c.601C>A	XP_011523946.1:p.Pro201Thr
XM_011525645.1:c.421C>A	XP_011523947.1:p.Pro141Thr
XM_011525646.1:c.985C>A	XP_011523948.1:p.Pro329Thr
XM_011525647.1:c.985C>A	XP_011523949.1:p.Pro329Thr
XR_430039.1:n.1174C>A
XR_935054.1:n.1174C>A
XR_935055.1:n.1174C>A
XM_011525643.2:c.985C>A	XP_011523945.1:p.Pro329Thr
XM_017025684.1:c.421C>A	XP_016881173.1:p.Pro141Thr
XR_001753172.1:n.1174C>A
XR_001753173.1:n.1174C>A
XR_001753174.1:n.1174C>A
XR_001753175.1:n.1174C>A
XR_001753176.1:n.1174C>A
XR_001753177.1:n.1174C>A
XR_001753178.1:n.1174C>A
XR_001753179.1:n.1174C>A
XR_935055.2:n.1174C>A
NM_015295.3:c.985C>A MANE Select	NP_056110.2:p.Pro329Thr