Canonical Allele Identifier: CA8870691
Gene: SMCHD1 HGNC NCBI

Linked Data

dbSNP Id: rs766297366
gnomAD v2: 18-2697792-A-G
gnomAD v3: 18-2697794-A-G
gnomAD v4: 18-2697794-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.2697794A>G , CM000680.2:g.2697794A>G GRCh38
NC_000018.9:g.2697792A>G , CM000680.1:g.2697792A>G GRCh37
NC_000018.8:g.2687792A>G NCBI36
NG_031972.1:g.46907A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684915.1:n.1289-37A>G
ENST00000688342.1:c.1132-37A>G ENSP00000508422.1:n.1132-37A>G
ENST00000693213.1:n.410-37A>G
ENST00000320876.11:c.1132-37A>G MANE Select ENSP00000326603.7:n.1132-37A>G
ENST00000320876.10:c.1132-37A>G ENSP00000326603.6:n.1132-37A>G
NM_015295.2:c.1132-37A>G NP_056110.2:n.1132-37A>G
XM_011525642.1:c.1132-37A>G XP_011523944.1:n.1132-37A>G
XM_011525643.1:c.1132-37A>G XP_011523945.1:n.1132-37A>G
XM_011525644.1:c.748-37A>G XP_011523946.1:n.748-37A>G
XM_011525645.1:c.568-37A>G XP_011523947.1:n.568-37A>G
XM_011525646.1:c.1132-37A>G XP_011523948.1:n.1132-37A>G
XM_011525647.1:c.1132-37A>G XP_011523949.1:n.1132-37A>G
XR_430039.1:n.1321-37A>G
XR_935054.1:n.1321-37A>G
XR_935055.1:n.1321-37A>G
XM_011525643.2:c.1132-37A>G XP_011523945.1:n.1132-37A>G
XM_017025684.1:c.568-37A>G XP_016881173.1:n.568-37A>G
XR_001753172.1:n.1321-37A>G
XR_001753173.1:n.1321-37A>G
XR_001753174.1:n.1321-37A>G
XR_001753175.1:n.1321-37A>G
XR_001753176.1:n.1321-37A>G
XR_001753177.1:n.1321-37A>G
XR_001753178.1:n.1321-37A>G
XR_001753179.1:n.1321-37A>G
XR_935055.2:n.1321-37A>G
NM_015295.3:c.1132-37A>G MANE Select NP_056110.2:n.1132-37A>G