Canonical Allele Identifier: CA455779780

Gene: SBDS

Linked Data

• MyVariant Identifiers: chr7:g.66453466G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66988479G>T , CM000669.2:g.66988479G>T	GRCh38
NC_000007.13:g.66453466G>T , CM000669.1:g.66453466G>T	GRCh37
NC_000007.12:g.66090901G>T	NCBI36
NG_007277.1:g.12123C>A , LRG_104:g.12123C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000414306.6:c.*376C>A	ENSP00000394586.1:n.*376C>A
ENST00000697860.1:n.612C>A
ENST00000697861.1:c.444C>A	ENSP00000513460.1:p.Gly148=
ENST00000697862.1:c.*86C>A	ENSP00000513461.1:n.*86C>A
ENST00000697863.1:c.588C>A	ENSP00000513462.1:p.Gly196=
ENST00000697864.1:n.1789C>A
ENST00000697865.1:c.588C>A	ENSP00000513463.1:p.Gly196=
ENST00000697866.1:c.327C>A	ENSP00000513464.1:p.Gly109=
ENST00000697867.1:c.623C>A
ENST00000697868.1:c.*409C>A	ENSP00000513466.1:n.*409C>A
ENST00000697897.1:c.645C>A	ENSP00000513469.1:p.Gly215=
ENST00000246868.7:c.645C>A MANE Select	ENSP00000246868.2:p.Gly215=
ENST00000246868.6:c.645C>A	ENSP00000246868.2:p.Gly215=
ENST00000414306.5:c.*376C>A	ENSP00000394586.1:n.*376C>A
ENST00000617799.1:c.645C>A	ENSP00000483040.1:p.Gly215=
NM_016038.2:c.645C>A , LRG_104t1:c.645C>A	NP_057122.2:p.Gly215=
NM_016038.3:c.645C>A	NP_057122.2:p.Gly215=
NM_016038.4:c.645C>A MANE Select	NP_057122.2:p.Gly215=