Canonical Allele Identifier: CA455779711

Gene: SBDS

Linked Data

• gnomAD v4: 7-66988377-A-G
• MyVariant Identifiers: chr7:g.66453364A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66988377A>G , CM000669.2:g.66988377A>G	GRCh38
NC_000007.13:g.66453364A>G , CM000669.1:g.66453364A>G	GRCh37
NC_000007.12:g.66090799A>G	NCBI36
NG_007277.1:g.12225T>C , LRG_104:g.12225T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000414306.6:c.*478T>C	ENSP00000394586.1:n.*478T>C
ENST00000697860.1:n.714T>C
ENST00000697861.1:c.546T>C	ENSP00000513460.1:p.Phe182=
ENST00000697862.1:c.*188T>C	ENSP00000513461.1:n.*188T>C
ENST00000697863.1:c.690T>C	ENSP00000513462.1:p.Phe230=
ENST00000697864.1:n.1891T>C
ENST00000697865.1:c.690T>C	ENSP00000513463.1:p.Phe230=
ENST00000697866.1:c.429T>C	ENSP00000513464.1:p.Phe143=
ENST00000697867.1:c.725T>C
ENST00000697868.1:c.*511T>C	ENSP00000513466.1:n.*511T>C
ENST00000697897.1:c.747T>C	ENSP00000513469.1:p.Phe249=
ENST00000246868.7:c.747T>C MANE Select	ENSP00000246868.2:p.Phe249=
ENST00000246868.6:c.747T>C	ENSP00000246868.2:p.Phe249=
ENST00000414306.5:c.*478T>C	ENSP00000394586.1:n.*478T>C
ENST00000617799.1:c.747T>C	ENSP00000483040.1:p.Phe249=
NM_016038.2:c.747T>C , LRG_104t1:c.747T>C	NP_057122.2:p.Phe249=
NM_016038.3:c.747T>C	NP_057122.2:p.Phe249=
NM_016038.4:c.747T>C MANE Select	NP_057122.2:p.Phe249=