Canonical Allele Identifier: CA360999338

Gene: SAR1B

Linked Data

• MyVariant Identifiers: chr5:g.133942650T>C (hg19) ; chr5:g.134606960T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134606960T>C , CM000667.2:g.134606960T>C	GRCh38
NC_000005.9:g.133942650T>C , CM000667.1:g.133942650T>C	GRCh37
NC_000005.8:g.133970549T>C	NCBI36
NG_017002.1:g.30884A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402673.7:c.587A>G MANE Select	ENSP00000385432.2:p.Tyr196Cys
ENST00000402673.6:c.587A>G	ENSP00000385432.2:p.Tyr196Cys
ENST00000439578.5:c.587A>G	ENSP00000404997.1:p.Tyr196Cys
ENST00000502539.5:c.383A>G	ENSP00000426335.1:p.Tyr128Cys
ENST00000507419.5:c.383A>G	ENSP00000425339.1:p.Tyr128Cys
ENST00000508363.5:n.2556A>G
ENST00000509937.5:c.383A>G	ENSP00000424673.1:p.Tyr128Cys
NM_001033503.2:c.587A>G	NP_001028675.1:p.Tyr196Cys
NM_016103.3:c.587A>G	NP_057187.1:p.Tyr196Cys
NM_016103.4:c.587A>G MANE Select	NP_057187.1:p.Tyr196Cys
NM_001033503.3:c.587A>G	NP_001028675.1:p.Tyr196Cys