Canonical Allele Identifier: CA361003297

Gene: SAR1B

Linked Data

• MyVariant Identifiers: chr5:g.133956622C>T (hg19) ; chr5:g.134620932C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134620932C>T , CM000667.2:g.134620932C>T	GRCh38
NC_000005.9:g.133956622C>T , CM000667.1:g.133956622C>T	GRCh37
NC_000005.8:g.133984521C>T	NCBI36
NG_017002.1:g.16912G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000402673.7:c.178+1G>A MANE Select	ENSP00000385432.2:n.178+1G>A
ENST00000402673.6:c.178+1G>A	ENSP00000385432.2:n.178+1G>A
ENST00000439578.5:c.178+1G>A	ENSP00000404997.1:n.178+1G>A
ENST00000502286.1:c.178+1G>A	ENSP00000423005.1:n.178+1G>A
ENST00000503318.5:c.178+1G>A	ENSP00000425367.1:n.178+1G>A
ENST00000505758.5:c.178+1G>A	ENSP00000425466.1:n.178+1G>A
ENST00000507419.5:c.-149+1G>A	ENSP00000425339.1:n.-149+1G>A
NM_001033503.2:c.178+1G>A	NP_001028675.1:n.178+1G>A
NM_016103.3:c.178+1G>A	NP_057187.1:n.178+1G>A
NM_016103.4:c.178+1G>A MANE Select	NP_057187.1:n.178+1G>A
NM_001033503.3:c.178+1G>A	NP_001028675.1:n.178+1G>A