Canonical Allele Identifier: CA2578412442

Gene: SAR1B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134606871A>G , CM000667.2:g.134606871A>G	GRCh38
NC_000005.9:g.133942561A>G , CM000667.1:g.133942561A>G	GRCh37
NC_000005.8:g.133970460A>G	NCBI36
NG_017002.1:g.30973T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402673.7:c.*79T>C MANE Select	ENSP00000385432.2:n.*79T>C
ENST00000402673.6:c.*79T>C	ENSP00000385432.2:n.*79T>C
ENST00000439578.5:c.*79T>C	ENSP00000404997.1:n.*79T>C
ENST00000502539.5:c.*79T>C	ENSP00000426335.1:n.*79T>C
ENST00000507419.5:c.*79T>C	ENSP00000425339.1:n.*79T>C
ENST00000508363.5:n.2645T>C
NM_001033503.2:c.*79T>C	NP_001028675.1:n.*79T>C
NM_016103.3:c.*79T>C	NP_057187.1:n.*79T>C
NM_016103.4:c.*79T>C MANE Select	NP_057187.1:n.*79T>C
NM_001033503.3:c.*79T>C	NP_001028675.1:n.*79T>C