Canonical Allele Identifier: CA455780153
Gene: SBDS HGNC NCBI

Linked Data

dbSNP Id: rs1197664803
gnomAD v2: 7-66458399-C-T
gnomAD v4: 7-66993412-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66993412C>T , CM000669.2:g.66993412C>T GRCh38
NC_000007.13:g.66458399C>T , CM000669.1:g.66458399C>T GRCh37
NC_000007.12:g.66095834C>T NCBI36
NG_007277.1:g.7190G>A , LRG_104:g.7190G>A
NG_033069.1:g.1608C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000414306.6:c.256G>A ENSP00000394586.1:p.Asp86Asn
ENST00000697860.1:n.231G>A
ENST00000697861.1:c.258+800G>A ENSP00000513460.1:n.258+800G>A
ENST00000697862.1:c.264G>A ENSP00000513461.1:p.Leu88=
ENST00000697863.1:c.207G>A ENSP00000513462.1:p.Leu69=
ENST00000697864.1:n.1408G>A
ENST00000697865.1:c.207G>A ENSP00000513463.1:p.Leu69=
ENST00000697866.1:c.-55G>A ENSP00000513464.1:n.-55G>A
ENST00000697867.1:c.104G>A
ENST00000697868.1:c.*28G>A ENSP00000513466.1:n.*28G>A
ENST00000697869.1:c.200G>A ENSP00000513467.1:p.Ter67=
ENST00000697897.1:c.264G>A ENSP00000513469.1:p.Leu88=
ENST00000246868.7:c.264G>A MANE Select ENSP00000246868.2:p.Leu88=
ENST00000246868.6:c.264G>A ENSP00000246868.2:p.Leu88=
ENST00000414306.5:c.256G>A ENSP00000394586.1:p.Asp86Asn
ENST00000463579.1:n.153G>A
ENST00000490953.5:n.405G>A
ENST00000617799.1:c.264G>A ENSP00000483040.1:p.Leu88=
NM_016038.2:c.264G>A , LRG_104t1:c.264G>A NP_057122.2:p.Leu88=
NM_016038.3:c.264G>A NP_057122.2:p.Leu88=
NM_016038.4:c.264G>A MANE Select NP_057122.2:p.Leu88=