Canonical Allele Identifier: CA360999607

Gene: SAR1B

Linked Data

• MyVariant Identifiers: chr5:g.133942702T>C (hg19) ; chr5:g.134607012T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134607012T>C , CM000667.2:g.134607012T>C	GRCh38
NC_000005.9:g.133942702T>C , CM000667.1:g.133942702T>C	GRCh37
NC_000005.8:g.133970601T>C	NCBI36
NG_017002.1:g.30832A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402673.7:c.535A>G MANE Select	ENSP00000385432.2:p.Ser179Gly
ENST00000402673.6:c.535A>G	ENSP00000385432.2:p.Ser179Gly
ENST00000439578.5:c.535A>G	ENSP00000404997.1:p.Ser179Gly
ENST00000502539.5:c.331A>G	ENSP00000426335.1:p.Ser111Gly
ENST00000503318.5:c.*258A>G	ENSP00000425367.1:n.*258A>G
ENST00000507419.5:c.331A>G	ENSP00000425339.1:p.Ser111Gly
ENST00000508363.5:n.2504A>G
ENST00000509730.5:c.331A>G	ENSP00000423197.1:p.Ser111Gly
ENST00000509937.5:c.331A>G	ENSP00000424673.1:p.Ser111Gly
NM_001033503.2:c.535A>G	NP_001028675.1:p.Ser179Gly
NM_016103.3:c.535A>G	NP_057187.1:p.Ser179Gly
NM_016103.4:c.535A>G MANE Select	NP_057187.1:p.Ser179Gly
NM_001033503.3:c.535A>G	NP_001028675.1:p.Ser179Gly