Canonical Allele Identifier: CA2683133627
Gene: SBDS HGNC NCBI

Linked Data

gnomAD v4: 7-66993470-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66993470T>C , CM000669.2:g.66993470T>C GRCh38
NC_000007.13:g.66458457T>C , CM000669.1:g.66458457T>C GRCh37
NC_000007.12:g.66095892T>C NCBI36
NG_007277.1:g.7132A>G , LRG_104:g.7132A>G
NG_033069.1:g.1666T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000414306.6:c.251-53A>G ENSP00000394586.1:n.251-53A>G
ENST00000697860.1:n.226-53A>G
ENST00000697861.1:c.258+742A>G ENSP00000513460.1:n.258+742A>G
ENST00000697862.1:c.259-53A>G ENSP00000513461.1:n.259-53A>G
ENST00000697863.1:c.202-53A>G ENSP00000513462.1:n.202-53A>G
ENST00000697864.1:n.1403-53A>G
ENST00000697865.1:c.202-53A>G ENSP00000513463.1:n.202-53A>G
ENST00000697866.1:c.-60-53A>G ENSP00000513464.1:n.-60-53A>G
ENST00000697867.1:c.99-53A>G
ENST00000697868.1:c.*23-53A>G ENSP00000513466.1:n.*23-53A>G
ENST00000697869.1:c.195-53A>G ENSP00000513467.1:n.195-53A>G
ENST00000697897.1:c.259-53A>G ENSP00000513469.1:n.259-53A>G
ENST00000246868.7:c.259-53A>G MANE Select ENSP00000246868.2:n.259-53A>G
ENST00000246868.6:c.259-53A>G ENSP00000246868.2:n.259-53A>G
ENST00000414306.5:c.251-53A>G ENSP00000394586.1:n.251-53A>G
ENST00000463579.1:n.148-53A>G
ENST00000490953.5:n.400-53A>G
ENST00000617799.1:c.259-53A>G ENSP00000483040.1:n.259-53A>G
NM_016038.2:c.259-53A>G , LRG_104t1:c.259-53A>G NP_057122.2:n.259-53A>G
NM_016038.3:c.259-53A>G NP_057122.2:n.259-53A>G
NM_016038.4:c.259-53A>G MANE Select NP_057122.2:n.259-53A>G