Canonical Allele Identifier: CA2839904230

Gene: SAR1B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134606891A>C , CM000667.2:g.134606891A>C	GRCh38
NC_000005.9:g.133942581A>C , CM000667.1:g.133942581A>C	GRCh37
NC_000005.8:g.133970480A>C	NCBI36
NG_017002.1:g.30953T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402673.7:c.*59T>G MANE Select	ENSP00000385432.2:n.*59T>G
ENST00000402673.6:c.*59T>G	ENSP00000385432.2:n.*59T>G
ENST00000439578.5:c.*59T>G	ENSP00000404997.1:n.*59T>G
ENST00000502539.5:c.*59T>G	ENSP00000426335.1:n.*59T>G
ENST00000507419.5:c.*59T>G	ENSP00000425339.1:n.*59T>G
ENST00000508363.5:n.2625T>G
NM_001033503.2:c.*59T>G	NP_001028675.1:n.*59T>G
NM_016103.3:c.*59T>G	NP_057187.1:n.*59T>G
NM_016103.4:c.*59T>G MANE Select	NP_057187.1:n.*59T>G
NM_001033503.3:c.*59T>G	NP_001028675.1:n.*59T>G