Canonical Allele Identifier: CA367650708

Gene: SBDS

Linked Data

• MyVariant Identifiers: chr7:g.66458382T>C (hg19) ; chr7:g.66993395T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66993395T>C , CM000669.2:g.66993395T>C	GRCh38
NC_000007.13:g.66458382T>C , CM000669.1:g.66458382T>C	GRCh37
NC_000007.12:g.66095817T>C	NCBI36
NG_007277.1:g.7207A>G , LRG_104:g.7207A>G
NG_033069.1:g.1591T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414306.6:c.*12A>G	ENSP00000394586.1:n.*12A>G
ENST00000697860.1:n.248A>G
ENST00000697861.1:c.258+817A>G	ENSP00000513460.1:n.258+817A>G
ENST00000697862.1:c.281A>G	ENSP00000513461.1:p.Gln94Arg
ENST00000697863.1:c.224A>G	ENSP00000513462.1:p.Gln75Arg
ENST00000697864.1:n.1425A>G
ENST00000697865.1:c.224A>G	ENSP00000513463.1:p.Gln75Arg
ENST00000697866.1:c.-38A>G	ENSP00000513464.1:n.-38A>G
ENST00000697867.1:c.121A>G
ENST00000697868.1:c.*45A>G	ENSP00000513466.1:n.*45A>G
ENST00000697869.1:c.*16A>G	ENSP00000513467.1:n.*16A>G
ENST00000697897.1:c.281A>G	ENSP00000513469.1:p.Gln94Arg
ENST00000246868.7:c.281A>G MANE Select	ENSP00000246868.2:p.Gln94Arg
ENST00000246868.6:c.281A>G	ENSP00000246868.2:p.Gln94Arg
ENST00000414306.5:c.*12A>G	ENSP00000394586.1:n.*12A>G
ENST00000463579.1:n.170A>G
ENST00000490953.5:n.422A>G
ENST00000617799.1:c.281A>G	ENSP00000483040.1:p.Gln94Arg
NM_016038.2:c.281A>G , LRG_104t1:c.281A>G	NP_057122.2:p.Gln94Arg
NM_016038.3:c.281A>G	NP_057122.2:p.Gln94Arg
NM_016038.4:c.281A>G MANE Select	NP_057122.2:p.Gln94Arg