Canonical Allele Identifier: CA1584149872
Gene: SAR1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.134606919C= , CM000667.2:g.134606919C= GRCh38
NC_000005.9:g.133942609C= , CM000667.1:g.133942609C= GRCh37
NC_000005.8:g.133970508C= NCBI36
NG_017002.1:g.30925G=

Transcript Alleles

HGVS Amino-acid change
ENST00000402673.7:c.*31G= MANE Select ENSP00000385432.2:n.*31G=
ENST00000402673.6:c.*31G= ENSP00000385432.2:n.*31G=
ENST00000439578.5:c.*31G= ENSP00000404997.1:n.*31G=
ENST00000502539.5:c.*31G= ENSP00000426335.1:n.*31G=
ENST00000507419.5:c.*31G= ENSP00000425339.1:n.*31G=
ENST00000508363.5:n.2597G=
NM_001033503.2:c.*31G= NP_001028675.1:n.*31G=
NM_016103.3:c.*31G= NP_057187.1:n.*31G=
NM_016103.4:c.*31G= MANE Select NP_057187.1:n.*31G=
NM_001033503.3:c.*31G= NP_001028675.1:n.*31G=