Canonical Allele Identifier: CA2640807361
Gene: SMCHD1 HGNC NCBI

Linked Data

gnomAD v4: 18-2667050-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.2667050C>A , CM000680.2:g.2667050C>A GRCh38
NC_000018.9:g.2667049C>A , CM000680.1:g.2667049C>A GRCh37
NC_000018.8:g.2657049C>A NCBI36
NG_031972.1:g.16164C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684915.1:n.581+19C>A
ENST00000688342.1:c.424+19C>A ENSP00000508422.1:n.424+19C>A
ENST00000320876.11:c.424+19C>A MANE Select ENSP00000326603.7:n.424+19C>A
ENST00000320876.10:c.424+19C>A ENSP00000326603.6:n.424+19C>A
NM_015295.2:c.424+19C>A NP_056110.2:n.424+19C>A
XM_011525642.1:c.424+19C>A XP_011523944.1:n.424+19C>A
XM_011525643.1:c.424+19C>A XP_011523945.1:n.424+19C>A
XM_011525644.1:c.40+19C>A XP_011523946.1:n.40+19C>A
XM_011525645.1:c.-319+19C>A XP_011523947.1:n.-319+19C>A
XM_011525646.1:c.424+19C>A XP_011523948.1:n.424+19C>A
XM_011525647.1:c.424+19C>A XP_011523949.1:n.424+19C>A
XR_430039.1:n.613+19C>A
XR_935054.1:n.613+19C>A
XR_935055.1:n.613+19C>A
XM_011525643.2:c.424+19C>A XP_011523945.1:n.424+19C>A
XM_017025684.1:c.-319+19C>A XP_016881173.1:n.-319+19C>A
XR_001753172.1:n.613+19C>A
XR_001753173.1:n.613+19C>A
XR_001753174.1:n.613+19C>A
XR_001753175.1:n.613+19C>A
XR_001753176.1:n.613+19C>A
XR_001753177.1:n.613+19C>A
XR_001753178.1:n.613+19C>A
XR_001753179.1:n.613+19C>A
XR_935055.2:n.613+19C>A
NM_015295.3:c.424+19C>A MANE Select NP_056110.2:n.424+19C>A