Canonical Allele Identifier: CA2683133623
Gene: SBDS HGNC NCBI

Linked Data

gnomAD v4: 7-66993468-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66993468A>C , CM000669.2:g.66993468A>C GRCh38
NC_000007.13:g.66458455A>C , CM000669.1:g.66458455A>C GRCh37
NC_000007.12:g.66095890A>C NCBI36
NG_007277.1:g.7134T>G , LRG_104:g.7134T>G
NG_033069.1:g.1664A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000414306.6:c.251-51T>G ENSP00000394586.1:n.251-51T>G
ENST00000697860.1:n.226-51T>G
ENST00000697861.1:c.258+744T>G ENSP00000513460.1:n.258+744T>G
ENST00000697862.1:c.259-51T>G ENSP00000513461.1:n.259-51T>G
ENST00000697863.1:c.202-51T>G ENSP00000513462.1:n.202-51T>G
ENST00000697864.1:n.1403-51T>G
ENST00000697865.1:c.202-51T>G ENSP00000513463.1:n.202-51T>G
ENST00000697866.1:c.-60-51T>G ENSP00000513464.1:n.-60-51T>G
ENST00000697867.1:c.99-51T>G
ENST00000697868.1:c.*23-51T>G ENSP00000513466.1:n.*23-51T>G
ENST00000697869.1:c.195-51T>G ENSP00000513467.1:n.195-51T>G
ENST00000697897.1:c.259-51T>G ENSP00000513469.1:n.259-51T>G
ENST00000246868.7:c.259-51T>G MANE Select ENSP00000246868.2:n.259-51T>G
ENST00000246868.6:c.259-51T>G ENSP00000246868.2:n.259-51T>G
ENST00000414306.5:c.251-51T>G ENSP00000394586.1:n.251-51T>G
ENST00000463579.1:n.148-51T>G
ENST00000490953.5:n.400-51T>G
ENST00000617799.1:c.259-51T>G ENSP00000483040.1:n.259-51T>G
NM_016038.2:c.259-51T>G , LRG_104t1:c.259-51T>G NP_057122.2:n.259-51T>G
NM_016038.3:c.259-51T>G NP_057122.2:n.259-51T>G
NM_016038.4:c.259-51T>G MANE Select NP_057122.2:n.259-51T>G