Canonical Allele Identifier: CA367643967

Gene: SBDS

Linked Data

• MyVariant Identifiers: chr7:g.66453365A>G (hg19) ; chr7:g.66988378A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66988378A>G , CM000669.2:g.66988378A>G	GRCh38
NC_000007.13:g.66453365A>G , CM000669.1:g.66453365A>G	GRCh37
NC_000007.12:g.66090800A>G	NCBI36
NG_007277.1:g.12224T>C , LRG_104:g.12224T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000414306.6:c.*477T>C	ENSP00000394586.1:n.*477T>C
ENST00000697860.1:n.713T>C
ENST00000697861.1:c.545T>C	ENSP00000513460.1:p.Phe182Ser
ENST00000697862.1:c.*187T>C	ENSP00000513461.1:n.*187T>C
ENST00000697863.1:c.689T>C	ENSP00000513462.1:p.Phe230Ser
ENST00000697864.1:n.1890T>C
ENST00000697865.1:c.689T>C	ENSP00000513463.1:p.Phe230Ser
ENST00000697866.1:c.428T>C	ENSP00000513464.1:p.Phe143Ser
ENST00000697867.1:c.724T>C
ENST00000697868.1:c.*510T>C	ENSP00000513466.1:n.*510T>C
ENST00000697897.1:c.746T>C	ENSP00000513469.1:p.Phe249Ser
ENST00000246868.7:c.746T>C MANE Select	ENSP00000246868.2:p.Phe249Ser
ENST00000246868.6:c.746T>C	ENSP00000246868.2:p.Phe249Ser
ENST00000414306.5:c.*477T>C	ENSP00000394586.1:n.*477T>C
ENST00000617799.1:c.746T>C	ENSP00000483040.1:p.Phe249Ser
NM_016038.2:c.746T>C , LRG_104t1:c.746T>C	NP_057122.2:p.Phe249Ser
NM_016038.3:c.746T>C	NP_057122.2:p.Phe249Ser
NM_016038.4:c.746T>C MANE Select	NP_057122.2:p.Phe249Ser