Canonical Allele Identifier: CA038798

Gene: DSC2

Linked Data

• ClinVar Variation Id: 950426
• ClinVar RCV Id: RCV001222130 ; RCV004010743
• dbSNP Id: rs774025474
• ExAC: 18:28669483 C / A
• gnomAD v2: 18-28669483-C-A
• gnomAD v4: 18-31089520-C-A
• MyVariant Identifiers: chr18:g.28669483C>A (hg19) ; chr18:g.31089520C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31089520C>A , CM000680.2:g.31089520C>A	GRCh38
NC_000018.9:g.28669483C>A , CM000680.1:g.28669483C>A	GRCh37
NC_000018.8:g.26923481C>A	NCBI36
NG_008208.2:g.17906G>T , LRG_400:g.17906G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.120G>T	ENSP00000507826.1:p.Arg40=
ENST00000251081.8:c.549G>T	ENSP00000251081.6:p.Arg183=
ENST00000280904.11:c.549G>T MANE Select	ENSP00000280904.6:p.Arg183=
ENST00000648081.1:c.120G>T	ENSP00000497441.1:p.Arg40=
ENST00000251081.6:c.549G>T	ENSP00000251081.6:p.Arg183=
ENST00000280904.10:c.549G>T	ENSP00000280904.6:p.Arg183=
NM_004949.4:c.549G>T	NP_004940.1:p.Arg183=
NM_024422.4:c.549G>T	NP_077740.1:p.Arg183=
XM_005258206.3:c.120G>T	XP_005258263.1:p.Arg40=
XM_005258206.4:c.120G>T	XP_005258263.1:p.Arg40=
NM_004949.5:c.549G>T	NP_004940.1:p.Arg183=
NM_024422.6:c.549G>T MANE Select	NP_077740.1:p.Arg183=