Canonical Allele Identifier: CA502670779

Gene: SMCHD1

Linked Data

• dbSNP Id: rs1328051296
• gnomAD v2: 18-2667020-A-G
• gnomAD v4: 18-2667021-A-G
• MyVariant Identifiers: chr18:g.2667020A>G (hg19) ; chr18:g.2667021A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2667021A>G , CM000680.2:g.2667021A>G	GRCh38
NC_000018.9:g.2667020A>G , CM000680.1:g.2667020A>G	GRCh37
NC_000018.8:g.2657020A>G	NCBI36
NG_031972.1:g.16135A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684915.1:n.571A>G
ENST00000688342.1:c.414A>G	ENSP00000508422.1:p.Gln138=
ENST00000320876.11:c.414A>G MANE Select	ENSP00000326603.7:p.Gln138=
ENST00000320876.10:c.414A>G	ENSP00000326603.6:p.Gln138=
NM_015295.2:c.414A>G	NP_056110.2:p.Gln138=
XM_011525642.1:c.414A>G	XP_011523944.1:p.Gln138=
XM_011525643.1:c.414A>G	XP_011523945.1:p.Gln138=
XM_011525644.1:c.30A>G	XP_011523946.1:p.Gln10=
XM_011525645.1:c.-329A>G	XP_011523947.1:n.-329A>G
XM_011525646.1:c.414A>G	XP_011523948.1:p.Gln138=
XM_011525647.1:c.414A>G	XP_011523949.1:p.Gln138=
XR_430039.1:n.603A>G
XR_935054.1:n.603A>G
XR_935055.1:n.603A>G
XM_011525643.2:c.414A>G	XP_011523945.1:p.Gln138=
XM_017025684.1:c.-329A>G	XP_016881173.1:n.-329A>G
XR_001753172.1:n.603A>G
XR_001753173.1:n.603A>G
XR_001753174.1:n.603A>G
XR_001753175.1:n.603A>G
XR_001753176.1:n.603A>G
XR_001753177.1:n.603A>G
XR_001753178.1:n.603A>G
XR_001753179.1:n.603A>G
XR_935055.2:n.603A>G
NM_015295.3:c.414A>G MANE Select	NP_056110.2:p.Gln138=